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esv3782588

  • Study:estd192 (COSMIC)
  • Variant Type:tandem duplication
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:488,671

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 1196 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):28,110,231-28,598,901Question Mark
Overlapping variant regions from other studies: 1196 SVs from 71 studies. See in: genome view    
Submitted genomic25,690,195-26,178,865Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3782588RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1828,110,23128,110,25128,598,88128,598,901
esv3782588Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr1825,690,19525,690,21526,178,84526,178,865

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16608707tandem duplication2196701CuratedCurated85

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16608707RemappedPerfectNC_000018.10:g.(28
110231_28110251)_(
28598881_28598901)
dup
GRCh38.p12First PassNC_000018.10Chr1828,110,23128,110,25128,598,88128,598,901
essv16608707Submitted genomicNC_000018.9:g.(256
90195_25690215)_(2
6178845_26178865)d
up
GRCh37 (hg19)NC_000018.9Chr1825,690,19525,690,21526,178,84526,178,865

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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