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esv3815443

  • 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:166,066,633

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 348564 SVs from 156 studies. See in: genome view    
Remapped(Score: Good):14,333,723-180,400,355Question Mark
Overlapping variant regions from other studies: 347047 SVs from 156 studies. See in: genome view    
Submitted genomic14,660,218-180,369,490Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3815443RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr114,333,72314,333,723180,400,355180,400,355
esv3815443Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr114,660,21814,660,238180,369,470180,369,490

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16645353deletion2185820CuratedCurated525

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16645353RemappedGoodNC_000001.11:g.(14
333723_14333723)_(
180400355_18040035
5)del
GRCh38.p12First PassNC_000001.11Chr114,333,72314,333,723180,400,355180,400,355
essv16645353Submitted genomicNC_000001.10:g.(14
660218_14660238)_(
180369470_18036949
0)del
GRCh37 (hg19)NC_000001.10Chr114,660,21814,660,238180,369,470180,369,490

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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