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esv3770604

  • Study:estd192 (COSMIC)
  • Variant Type:tandem duplication
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,588

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 92 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):107,287,347-107,295,934Question Mark
Overlapping variant regions from other studies: 74 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):107,295,862-107,296,388Question Mark
Overlapping variant regions from other studies: 92 SVs from 33 studies. See in: genome view    
Submitted genomic107,829,969-107,838,556Question Mark
Overlapping variant regions from other studies: 74 SVs from 22 studies. See in: genome view    
Submitted genomic107,838,484-107,839,010Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv3770604RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1107,287,347107,295,934
esv3770604RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1107,295,862107,296,388
esv3770604Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1107,829,969107,838,556
esv3770604Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1107,838,484107,839,010

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16601003intrachromosomal translocation1126076CuratedCurated208
essv16641459intrachromosomal translocation1126076CuratedCurated208

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
essv16601003RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1107,287,347107,287,347-
essv16641459RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1107,295,862107,295,862-
essv16601003Submitted genomicGRCh37 (hg19)NC_000001.10Chr1107,829,969107,829,969-
essv16641459Submitted genomicGRCh37 (hg19)NC_000001.10Chr1107,838,484107,838,484-

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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