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nsv818594

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,908

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 482 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):8,725,599-8,728,506Question Mark
Overlapping variant regions from other studies: 256 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):4,623,629-4,626,536Question Mark
Overlapping variant regions from other studies: 482 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):8,583,109-8,586,016Question Mark
Overlapping variant regions from other studies: 7 SVs from 3 studies. See in: genome view    
Submitted genomic8,620,519-8,623,426Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv818594RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr88,725,5998,728,506
nsv818594RemappedPerfectGRCh38.p12PATCHESSecond PassNW_018654717.1Chr8|NW_01
8654717.1		4,623,6294,626,536
nsv818594RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr88,583,1098,586,016
nsv818594Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000008.9Chr88,620,5198,623,426

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1416252copy number lossNA12056SNP arrayProbe signal intensity26
nssv1416253copy number lossNA10851SNP arrayProbe signal intensity23

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1416252RemappedPerfectNW_018654717.1:g.(
?_4623629)_(462653
6_?)del		GRCh38.p12Second PassNW_018654717.1Chr8|NW_01
8654717.1		4,623,6294,626,536
nssv1416253RemappedPerfectNW_018654717.1:g.(
?_4623629)_(462653
6_?)del		GRCh38.p12Second PassNW_018654717.1Chr8|NW_01
8654717.1		4,623,6294,626,536
nssv1416252RemappedPerfectNC_000008.11:g.(?_
8725599)_(8728506_
?)del		GRCh38.p12First PassNC_000008.11Chr88,725,5998,728,506
nssv1416253RemappedPerfectNC_000008.11:g.(?_
8725599)_(8728506_
?)del		GRCh38.p12First PassNC_000008.11Chr88,725,5998,728,506
nssv1416252RemappedPerfectNC_000008.10:g.(?_
8583109)_(8586016_
?)del		GRCh37.p13First PassNC_000008.10Chr88,583,1098,586,016
nssv1416253RemappedPerfectNC_000008.10:g.(?_
8583109)_(8586016_
?)del		GRCh37.p13First PassNC_000008.10Chr88,583,1098,586,016
nssv1416252Submitted genomicNC_000008.9:g.(?_8
620519)_(8623426_?
)del		NCBI35 (hg17)NC_000008.9Chr88,620,5198,623,426
nssv1416253Submitted genomicNC_000008.9:g.(?_8
620519)_(8623426_?
)del		NCBI35 (hg17)NC_000008.9Chr88,620,5198,623,426

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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