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esv2668553

  • Variant Calls:22
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:25,109

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 271 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):6,198,518-6,223,626Question Mark
Overlapping variant regions from other studies: 271 SVs from 59 studies. See in: genome view    
Submitted genomic6,101,838-6,126,946Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv2668553RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr176,198,5186,223,626
esv2668553Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr176,101,8386,126,946

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5441331deletionSAMN00001182SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,509
essv5474977deletionSAMN00001102SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,259
essv5553076deletionSAMN00007818SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,316
essv5622316deletionSAMN00000571SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,271
essv5624100deletionSAMN00009250SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,377
essv5631209deletionSAMN00000414SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,260
essv5694209deletionSAMN00001149SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,599
essv5842469deletionSAMN00001180SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,453
essv5877031deletionSAMN00001173SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,274
essv5951360deletionSAMN00001685SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,589
essv5970710deletionSAMN00001181SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,016
essv5978734deletionSAMN00001629SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,430
essv6017336deletionSAMN00001150SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,706
essv6039421deletionSAMN00001137SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,647
essv6082165deletionSAMN00000574SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,208
essv6159047deletionSAMN00001183SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,354
essv6181108deletionSAMN00001117SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,366
essv6408429deletionSAMN00006534SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping915
essv6410556deletionSAMN00001131SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,611
essv6415542deletionSAMN00001164SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,515
essv6462658deletionSAMN00001140SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,625
essv6551687deletionSAMN00001138SequencingPaired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping1,561

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv5441331RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5474977RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5553076RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5622316RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5624100RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5631209RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5694209RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5842469RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5877031RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5951360RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5970710RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5978734RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv6017336RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv6039421RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv6082165RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv6159047RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv6181108RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv6408429RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv6410556RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv6415542RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv6462658RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv6551687RemappedPerfectNC_000017.11:g.619
8518_6223626delC
GRCh38.p12First PassNC_000017.11Chr176,198,5186,223,626
essv5441331Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv5474977Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv5553076Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv5622316Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv5624100Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv5631209Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv5694209Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv5842469Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv5877031Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv5951360Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv5970710Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv5978734Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv6017336Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv6039421Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv6082165Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv6159047Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv6181108Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv6408429Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv6410556Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv6415542Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv6462658Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946
essv6551687Submitted genomicNC_000017.10:g.610
1838_6126946delC
GRCh37 (hg19)NC_000017.10Chr176,101,8386,126,946

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv56312099SAMN00000414Oligo aCGHProbe signal intensityPass
essv56223169SAMN00000571Oligo aCGHProbe signal intensityPass
essv60821659SAMN00000574Oligo aCGHProbe signal intensityPass
essv54749779SAMN00001102Oligo aCGHProbe signal intensityPass
essv61811089SAMN00001117Oligo aCGHProbe signal intensityPass
essv64105569SAMN00001131Oligo aCGHProbe signal intensityPass
essv60394219SAMN00001137Oligo aCGHProbe signal intensityPass
essv65516879SAMN00001138Oligo aCGHProbe signal intensityPass
essv64626589SAMN00001140Oligo aCGHProbe signal intensityPass
essv56942099SAMN00001149Oligo aCGHProbe signal intensityPass
essv60173369SAMN00001150Oligo aCGHProbe signal intensityPass
essv64155429SAMN00001164Oligo aCGHProbe signal intensityPass
essv58770319SAMN00001173Oligo aCGHProbe signal intensityPass
essv58424699SAMN00001180Oligo aCGHProbe signal intensityPass
essv59707109SAMN00001181Oligo aCGHProbe signal intensityPass
essv54413319SAMN00001182Oligo aCGHProbe signal intensityPass
essv61590479SAMN00001183Oligo aCGHProbe signal intensityPass
essv59787349SAMN00001629Oligo aCGHProbe signal intensityPass
essv59513609SAMN00001685Oligo aCGHProbe signal intensityPass
essv64084299SAMN00006534Oligo aCGHProbe signal intensityPass
essv55530769SAMN00007818Oligo aCGHProbe signal intensityPass
essv56241009SAMN00009250Oligo aCGHProbe signal intensityPass
essv56312097SAMN00000414SNP arrayProbe signal intensityPass
essv56223167SAMN00000571SNP arrayProbe signal intensityPass
essv60821657SAMN00000574SNP arrayProbe signal intensityPass
essv54749777SAMN00001102SNP arrayProbe signal intensityPass
essv61811087SAMN00001117SNP arrayProbe signal intensityPass
essv64105567SAMN00001131SNP arrayProbe signal intensityPass
essv60394217SAMN00001137SNP arrayProbe signal intensityPass
essv65516877SAMN00001138SNP arrayProbe signal intensityPass
essv64626587SAMN00001140SNP arrayProbe signal intensityPass
essv56942097SAMN00001149SNP arrayProbe signal intensityPass
essv60173367SAMN00001150SNP arrayProbe signal intensityPass
essv64155427SAMN00001164SNP arrayProbe signal intensityPass
essv58770317SAMN00001173SNP arrayProbe signal intensityPass
essv58424697SAMN00001180SNP arrayProbe signal intensityPass
essv59707107SAMN00001181SNP arrayProbe signal intensityPass
essv54413317SAMN00001182SNP arrayProbe signal intensityPass
essv61590477SAMN00001183SNP arrayProbe signal intensityPass
essv59787347SAMN00001629SNP arrayProbe signal intensityPass
essv59513607SAMN00001685SNP arrayProbe signal intensityPass
essv64084297SAMN00006534SNP arrayProbe signal intensityPass
essv55530767SAMN00007818SNP arrayProbe signal intensityPass
essv56241007SAMN00009250SNP arrayProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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