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nsv6530819

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 19 studies. See in: genome view    
    Submitted genomic39,636,101-39,636,900Question Mark
    Overlapping variant regions from other studies: 114 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):40,126,741-40,127,540Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6530819Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1939,636,10139,636,900
    nsv6530819RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1940,126,74140,127,540

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18047890deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18047890Submitted genomicNC_000019.10:g.396
    36101_39636900del
    GRCh38 (hg38)NC_000019.10Chr1939,636,10139,636,900
    nssv18047890RemappedPerfectNC_000019.9:g.4012
    6741_40127540del
    GRCh37.p13First PassNC_000019.9Chr1940,126,74140,127,540

    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)
    nssv18047890<0.001137010
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