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esv3815827

  • 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:423

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 139 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):155,328,112-155,328,534Question Mark
Overlapping variant regions from other studies: 139 SVs from 42 studies. See in: genome view    
Submitted genomic156,249,264-156,249,686Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3815827RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4155,328,112155,328,132155,328,514155,328,534
esv3815827Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr4156,249,264156,249,284156,249,666156,249,686

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16645772deletion1842438CuratedCurated649

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16645772RemappedPerfectNC_000004.12:g.(15
5328112_155328132)
_(155328514_155328
534)del
GRCh38.p12First PassNC_000004.12Chr4155,328,112155,328,132155,328,514155,328,534
essv16645772Submitted genomicNC_000004.11:g.(15
6249264_156249284)
_(156249666_156249
686)del
GRCh37 (hg19)NC_000004.11Chr4156,249,264156,249,284156,249,666156,249,686

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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