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esv3803141

  • 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:702,826

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1801 SVs from 85 studies. See in: genome view    
Remapped(Score: Perfect):124,751,661-125,454,486Question Mark
Overlapping variant regions from other studies: 1801 SVs from 85 studies. See in: genome view    
Submitted genomic125,672,816-126,375,641Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3803141RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4124,751,661124,751,681125,454,466125,454,486
esv3803141Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr4125,672,816125,672,836126,375,621126,375,641

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16631597deletion2197223CuratedCurated122

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16631597RemappedPerfectNC_000004.12:g.(12
4751661_124751681)
_(125454466_125454
486)del		GRCh38.p12First PassNC_000004.12Chr4124,751,661124,751,681125,454,466125,454,486
essv16631597Submitted genomicNC_000004.11:g.(12
5672816_125672836)
_(126375621_126375
641)del		GRCh37 (hg19)NC_000004.11Chr4125,672,816125,672,836126,375,621126,375,641

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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