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esv3815794

  • Study:estd192 (COSMIC)
  • Variant Type:complex chromosomal rearrangement
  • Method Type:Curated
  • Submitted on:GRCh37
  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 137 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):83,288,004-83,288,004Question Mark
Overlapping variant regions from other studies: 91 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):93,624,949-93,624,949Question Mark
Overlapping variant regions from other studies: 137 SVs from 21 studies. See in: genome view    
Submitted genomic84,200,239-84,200,239Question Mark
Overlapping variant regions from other studies: 91 SVs from 15 studies. See in: genome view    
Submitted genomic94,637,177-94,637,177Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv3815794RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,288,00483,288,004
esv3815794RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr893,624,94993,624,949
esv3815794Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr884,200,23984,200,239
esv3815794Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr894,637,17794,637,177

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16645733deletion1669608CuratedCurated96

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
essv16645733RemappedPerfectNC_000008.11:g.832
88004delNC_000008.
11:g.93624949del		GRCh38.p12First PassNC_000008.11Chr883,288,00483,288,004
essv16645733RemappedPerfectNC_000008.11:g.832
88004delNC_000008.
11:g.93624949del		GRCh38.p12First PassNC_000008.11Chr893,624,94993,624,949
essv16645733Submitted genomic[NC_000008.10:g.84
200239del];[NC_000
008.10:g.94637177d
el]		GRCh37 (hg19)NC_000008.10Chr884,200,23984,200,239
essv16645733Submitted genomic[NC_000008.10:g.84
200239del];[NC_000
008.10:g.94637177d
el]		GRCh37 (hg19)NC_000008.10Chr894,637,17794,637,177

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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