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nsv6505349

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,276

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 22 studies. See in: genome view    
    Submitted genomic56,494,823-56,501,098Question Mark
    Overlapping variant regions from other studies: 92 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):56,528,735-56,535,010Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6505349Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1656,494,82356,501,098
    nsv6505349RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1656,528,73556,535,010

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18030224deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18030224Submitted genomicNC_000016.10:g.564
    94823_56501098del
    GRCh38 (hg38)NC_000016.10Chr1656,494,82356,501,098
    nssv18030224RemappedPerfectNC_000016.9:g.5652
    8735_56535010del
    GRCh37.p13First PassNC_000016.9Chr1656,528,73556,535,010

    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)
    nssv18030224<0.001139254
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