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nsv6457723

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:395,403

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 910 SVs from 63 studies. See in: genome view    
    Submitted genomic75,159,051-75,554,453Question Mark
    Overlapping variant regions from other studies: 912 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):74,870,096-75,265,498Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6457723Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1175,159,05175,554,453
    nsv6457723RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1174,870,09675,265,498

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18190212duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18190212Submitted genomicNC_000011.10:g.751
    59051_75554453dup
    GRCh38 (hg38)NC_000011.10Chr1175,159,05175,554,453
    nssv18190212RemappedPerfectNC_000011.9:g.7487
    0096_75265498dup
    GRCh37.p13First PassNC_000011.9Chr1174,870,09675,265,498

    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)
    nssv18190212<0.001139292
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