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esv3811992

  • 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:584,078

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 1938 SVs from 88 studies. See in: genome view    
Remapped(Score: Perfect):55,094,863-55,678,940Question Mark
Overlapping variant regions from other studies: 1938 SVs from 88 studies. See in: genome view    
Submitted genomic55,668,998-56,253,074Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3811992RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1355,094,86355,094,86355,678,94055,678,940
esv3811992Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1355,668,99855,669,01856,253,05456,253,074

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16641495deletion2196332CuratedCurated137

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16641495RemappedPerfectNC_000013.11:g.(55
094863_55094863)_(
55678940_55678940)
del
GRCh38.p12First PassNC_000013.11Chr1355,094,86355,094,86355,678,94055,678,940
essv16641495Submitted genomicNC_000013.10:g.(55
668998_55669018)_(
56253054_56253074)
del
GRCh37 (hg19)NC_000013.10Chr1355,668,99855,669,01856,253,05456,253,074

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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