U.S. flag

An official website of the United States government

nsv6504859

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,886

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 16 studies. See in: genome view    
    Submitted genomic80,717,597-80,719,482Question Mark
    Overlapping variant regions from other studies: 94 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):81,009,938-81,011,823Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6504859Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1580,717,59780,719,482
    nsv6504859RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1581,009,93881,011,823

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18026872deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18026872Submitted genomicNC_000015.10:g.807
    17597_80719482del
    GRCh38 (hg38)NC_000015.10Chr1580,717,59780,719,482
    nssv18026872RemappedPerfectNC_000015.9:g.8100
    9938_81011823del
    GRCh37.p13First PassNC_000015.9Chr1581,009,93881,011,823

    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)
    nssv18026872<0.001138934
    Support Center