U.S. flag

An official website of the United States government

nsv6518483

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:163

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 24 studies. See in: genome view    
    Submitted genomic40,670,432-40,670,594Question Mark
    Overlapping variant regions from other studies: 110 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):41,176,337-41,176,499Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6518483Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1940,670,43240,670,594
    nsv6518483RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1941,176,33741,176,499

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18047767deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18047767Submitted genomicNC_000019.10:g.406
    70432_40670594del
    GRCh38 (hg38)NC_000019.10Chr1940,670,43240,670,594
    nssv18047767RemappedPerfectNC_000019.9:g.4117
    6337_41176499del
    GRCh37.p13First PassNC_000019.9Chr1941,176,33741,176,499

    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)
    nssv18047767<0.001132604
    Support Center