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nsv6409723

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,093,674

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 13926 SVs from 120 studies. See in: genome view    
    Submitted genomic7,366,072-12,459,745Question Mark
    Overlapping variant regions from other studies: 13925 SVs from 120 studies. See in: genome view    
    Remapped(Score: Perfect):7,366,305-12,459,977Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6409723Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr67,366,07212,459,745
    nsv6409723RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr67,366,30512,459,977

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18223099duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18223099Submitted genomicNC_000006.12:g.736
    6072_12459745dup
    GRCh38 (hg38)NC_000006.12Chr67,366,07212,459,745
    nssv18223099RemappedPerfectNC_000006.11:g.736
    6305_12459977dup
    GRCh37.p13First PassNC_000006.11Chr67,366,30512,459,977

    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)
    nssv18223099<0.001139296
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