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nsv6519775

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,402

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 211 SVs from 41 studies. See in: genome view    
    Submitted genomic37,876,504-37,885,905Question Mark
    Overlapping variant regions from other studies: 211 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):38,367,144-38,376,545Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6519775Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1937,876,50437,885,905
    nsv6519775RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1938,367,14438,376,545

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18046685deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18046685Submitted genomicNC_000019.10:g.378
    76504_37885905del
    GRCh38 (hg38)NC_000019.10Chr1937,876,50437,885,905
    nssv18046685RemappedPerfectNC_000019.9:g.3836
    7144_38376545del
    GRCh37.p13First PassNC_000019.9Chr1938,367,14438,376,545

    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)
    nssv18046685<0.001139208
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