U.S. flag

An official website of the United States government

nsv6468231

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 33 studies. See in: genome view    
    Submitted genomic66,537,563-66,537,656Question Mark
    Overlapping variant regions from other studies: 115 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):66,305,034-66,305,127Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6468231Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1166,537,56366,537,656
    nsv6468231RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1166,305,03466,305,127

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17992577deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17992577Submitted genomicNC_000011.10:g.665
    37563_66537656del
    GRCh38 (hg38)NC_000011.10Chr1166,537,56366,537,656
    nssv17992577RemappedPerfectNC_000011.9:g.6630
    5034_66305127del
    GRCh37.p13First PassNC_000011.9Chr1166,305,03466,305,127

    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)
    nssv17992577<0.0011129024
    Support Center