U.S. flag

An official website of the United States government

esv3779073

  • Study:estd192 (COSMIC)
  • Variant Type:copy number variation
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:372,380

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 1041 SVs from 62 studies. See in: genome view    
Remapped(Score: Perfect):71,239,397-71,611,776Question Mark
Overlapping variant regions from other studies: 1041 SVs from 62 studies. See in: genome view    
Submitted genomic69,235,538-69,607,917Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3779073RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1771,239,39771,239,41771,611,75671,611,776
esv3779073Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr1769,235,53869,235,55869,607,89769,607,917

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16604795deletion2121109CuratedCurated40

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16604795RemappedPerfectNC_000017.11:g.(71
239397_71239417)_(
71611756_71611776)
del
GRCh38.p12First PassNC_000017.11Chr1771,239,39771,239,41771,611,75671,611,776
essv16604795Submitted genomicNC_000017.10:g.(69
235538_69235558)_(
69607897_69607917)
del
GRCh37 (hg19)NC_000017.10Chr1769,235,53869,235,55869,607,89769,607,917

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

Support Center