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esv3815826

  • 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: 138 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):128,654,691-128,654,691Question Mark
Overlapping variant regions from other studies: 169 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):75,986,267-75,986,267Question Mark
Overlapping variant regions from other studies: 6 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):99,969-99,969Question Mark
Overlapping variant regions from other studies: 138 SVs from 21 studies. See in: genome view    
Submitted genomic129,666,937-129,666,937Question Mark
Overlapping variant regions from other studies: 169 SVs from 24 studies. See in: genome view    
Submitted genomic76,560,403-76,560,403Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
esv3815826RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8128,654,691128,654,691
esv3815826RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1375,986,26775,986,267-
esv3815826RemappedPerfectGRCh38.p12ALT_REF_LOCI_1Second PassNT_187567.1Chr8|NT_18
7567.1		99,96999,969
esv3815826Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8129,666,937129,666,937
esv3815826Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1376,560,40376,560,403-

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv16645771interchromosomal translocation1126078CuratedCurated115

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
essv16645771RemappedPerfectGRCh38.p12Second PassNT_187567.1Chr8|NT_18
7567.1		99,96999,969not reported
essv16645771RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8128,654,691128,654,691not reported
essv16645771RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1375,986,26775,986,267-
essv16645771Submitted genomicGRCh37 (hg19)NC_000008.10Chr8129,666,937129,666,937not reported
essv16645771Submitted genomicGRCh37 (hg19)NC_000013.10Chr1376,560,40376,560,403-

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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