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esv18524

  • Variant Calls:7
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:18,367

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 459 SVs from 68 studies. See in: genome view    
Remapped(Score: Perfect):156,049,646-156,068,012Question Mark
Overlapping variant regions from other studies: 459 SVs from 68 studies. See in: genome view    
Remapped(Score: Perfect):155,476,656-155,495,022Question Mark
Overlapping variant regions from other studies: 211 SVs from 20 studies. See in: genome view    
Submitted genomic155,409,234-155,427,600Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv18524RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5156,049,646156,068,012
esv18524RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5155,476,656155,495,022
esv18524Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000005.8Chr5155,409,234155,427,600

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv35080copy number lossNA18502Oligo aCGHProbe signal intensity1,373
essv56704copy number lossNA12776Oligo aCGHProbe signal intensity1,114
essv49974copy number lossNA18517Oligo aCGHProbe signal intensity1,365
essv67403copy number lossNA12828Oligo aCGHProbe signal intensity1,072
essv62899copy number lossNA15510Oligo aCGHProbe signal intensity1,307
essv68165copy number lossNA18858Oligo aCGHProbe signal intensity1,507
essv39786copy number lossNA12287Oligo aCGHProbe signal intensity1,073

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv35080RemappedPerfectNC_000005.10:g.(?_
156049646)_(156061
890_?)del
GRCh38.p12First PassNC_000005.10Chr5156,049,646156,061,890
essv56704RemappedPerfectNC_000005.10:g.(?_
156049646)_(156061
890_?)del
GRCh38.p12First PassNC_000005.10Chr5156,049,646156,061,890
essv49974RemappedPerfectNC_000005.10:g.(?_
156049657)_(156061
890_?)del
GRCh38.p12First PassNC_000005.10Chr5156,049,657156,061,890
essv67403RemappedPerfectNC_000005.10:g.(?_
156049657)_(156068
012_?)del
GRCh38.p12First PassNC_000005.10Chr5156,049,657156,068,012
essv62899RemappedPerfectNC_000005.10:g.(?_
156049764)_(156061
890_?)del
GRCh38.p12First PassNC_000005.10Chr5156,049,764156,061,890
essv68165RemappedPerfectNC_000005.10:g.(?_
156050412)_(156061
890_?)del
GRCh38.p12First PassNC_000005.10Chr5156,050,412156,061,890
essv39786RemappedPerfectNC_000005.10:g.(?_
156050782)_(156068
012_?)del
GRCh38.p12First PassNC_000005.10Chr5156,050,782156,068,012
essv35080RemappedPerfectNC_000005.9:g.(?_1
55476656)_(1554889
00_?)del
GRCh37.p13First PassNC_000005.9Chr5155,476,656155,488,900
essv56704RemappedPerfectNC_000005.9:g.(?_1
55476656)_(1554889
00_?)del
GRCh37.p13First PassNC_000005.9Chr5155,476,656155,488,900
essv49974RemappedPerfectNC_000005.9:g.(?_1
55476667)_(1554889
00_?)del
GRCh37.p13First PassNC_000005.9Chr5155,476,667155,488,900
essv67403RemappedPerfectNC_000005.9:g.(?_1
55476667)_(1554950
22_?)del
GRCh37.p13First PassNC_000005.9Chr5155,476,667155,495,022
essv62899RemappedPerfectNC_000005.9:g.(?_1
55476774)_(1554889
00_?)del
GRCh37.p13First PassNC_000005.9Chr5155,476,774155,488,900
essv68165RemappedPerfectNC_000005.9:g.(?_1
55477422)_(1554889
00_?)del
GRCh37.p13First PassNC_000005.9Chr5155,477,422155,488,900
essv39786RemappedPerfectNC_000005.9:g.(?_1
55477792)_(1554950
22_?)del
GRCh37.p13First PassNC_000005.9Chr5155,477,792155,495,022
essv35080Submitted genomicNC_000005.8:g.(?_1
55409234)_(1554214
78_?)del
NCBI36 (hg18)NC_000005.8Chr5155,409,234155,421,478
essv56704Submitted genomicNC_000005.8:g.(?_1
55409234)_(1554214
78_?)del
NCBI36 (hg18)NC_000005.8Chr5155,409,234155,421,478
essv49974Submitted genomicNC_000005.8:g.(?_1
55409245)_(1554214
78_?)del
NCBI36 (hg18)NC_000005.8Chr5155,409,245155,421,478
essv67403Submitted genomicNC_000005.8:g.(?_1
55409245)_(1554276
00_?)del
NCBI36 (hg18)NC_000005.8Chr5155,409,245155,427,600
essv62899Submitted genomicNC_000005.8:g.(?_1
55409352)_(1554214
78_?)del
NCBI36 (hg18)NC_000005.8Chr5155,409,352155,421,478
essv68165Submitted genomicNC_000005.8:g.(?_1
55410000)_(1554214
78_?)del
NCBI36 (hg18)NC_000005.8Chr5155,410,000155,421,478
essv39786Submitted genomicNC_000005.8:g.(?_1
55410370)_(1554276
00_?)del
NCBI36 (hg18)NC_000005.8Chr5155,410,370155,427,600

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv397862NA12287Oligo aCGHProbe signal intensityPass
essv567042NA12776Oligo aCGHProbe signal intensityPass
essv674032NA12828Oligo aCGHProbe signal intensityPass
essv628992NA15510Oligo aCGHProbe signal intensityPass
essv350802NA18502Oligo aCGHProbe signal intensityPass
essv499742NA18517Oligo aCGHProbe signal intensityPass
essv681652NA18858Oligo aCGHProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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