U.S. flag

An official website of the United States government

esv3806158

  • Study:estd192 (COSMIC)
  • Variant Type:tandem duplication
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50,569,788

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 133952 SVs from 151 studies. See in: genome view    
Remapped(Score: Good):20,301,411-70,871,198Question Mark
Overlapping variant regions from other studies: 134090 SVs from 151 studies. See in: genome view    
Submitted genomic20,322,957-70,717,303Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3806158RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1120,301,41120,301,41170,871,19870,871,198
esv3806158Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1120,322,95720,322,97770,717,28370,717,303

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16634962tandem duplication2196242CuratedCurated225

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16634962RemappedGoodNC_000011.10:g.(20
301411_20301411)_(
70871198_70871198)
dup
GRCh38.p12First PassNC_000011.10Chr1120,301,41120,301,41170,871,19870,871,198
essv16634962Submitted genomicNC_000011.9:g.(203
22957_20322977)_(7
0717283_70717303)d
up
GRCh37 (hg19)NC_000011.9Chr1120,322,95720,322,97770,717,28370,717,303

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