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nsv6795434

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,299

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 154 SVs from 40 studies. See in: genome view    
    Submitted genomic6,647,143-6,663,441Question Mark
    Overlapping variant regions from other studies: 154 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):6,647,376-6,663,674Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6795434Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr66,647,1436,663,441
    nsv6795434RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr66,647,3766,663,674

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18527352deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18527352Submitted genomicNC_000006.12:g.664
    7143_6663441del
    GRCh38 (hg38)NC_000006.12Chr66,647,1436,663,441
    nssv18527352RemappedPerfectNC_000006.11:g.664
    7376_6663674del
    GRCh37.p13First PassNC_000006.11Chr66,647,3766,663,674

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv185273524e-061276262
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