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esv3760098

  • Study:estd192 (COSMIC)
  • Variant Type:tandem duplication
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,198,019

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 2629 SVs from 89 studies. See in: genome view    
Remapped(Score: Good):57,877,603-61,075,621Question Mark
Overlapping variant regions from other studies: 1390 SVs from 82 studies. See in: genome view    
Submitted genomic57,937,309-61,058,346Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv3760098RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr757,877,60357,877,60361,075,62161,075,621
esv3760098Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr757,937,30957,937,50961,058,14661,058,346

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16583641tandem duplication2196316CuratedCurated275

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv16583641RemappedGoodNC_000007.14:g.(57
877603_57877603)_(
61075621_61075621)
dup
GRCh38.p12First PassNC_000007.14Chr757,877,60357,877,60361,075,62161,075,621
essv16583641Submitted genomicNC_000007.13:g.(57
937309_57937509)_(
61058146_61058346)
dup
GRCh37 (hg19)NC_000007.13Chr757,937,30957,937,50961,058,14661,058,346

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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