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nsv5932060

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:836

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 85 SVs from 26 studies. See in: genome view    
Submitted genomic7,886,306-7,887,141Question Mark
Overlapping variant regions from other studies: 85 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):7,951,191-7,952,026Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5932060Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr197,886,3067,887,141
nsv5932060RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr197,951,1917,952,026

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17399682deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17399682Submitted genomicNC_000019.10:g.788
6306_7887141del
GRCh38 (hg38)NC_000019.10Chr197,886,3067,887,141
nssv17399682RemappedPerfectNC_000019.9:g.7951
191_7952026del
GRCh37.p13First PassNC_000019.9Chr197,951,1917,952,026

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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