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nsv6409255

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 29 studies. See in: genome view    
    Submitted genomic95,604,701-95,605,300Question Mark
    Overlapping variant regions from other studies: 118 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):96,052,577-96,053,176Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6409255Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr695,604,70195,605,300
    nsv6409255RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr696,052,57796,053,176

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18149809deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18149809Submitted genomicNC_000006.12:g.956
    04701_95605300del
    GRCh38 (hg38)NC_000006.12Chr695,604,70195,605,300
    nssv18149809RemappedPerfectNC_000006.11:g.960
    52577_96053176del
    GRCh37.p13First PassNC_000006.11Chr696,052,57796,053,176

    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)
    nssv18149809<0.0011137390
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