U.S. flag

An official website of the United States government

nsv6402177

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 23 studies. See in: genome view    
    Submitted genomic27,958,601-27,959,800Question Mark
    Overlapping variant regions from other studies: 92 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):27,926,379-27,927,578Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6402177Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr627,958,60127,959,800
    nsv6402177RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr627,926,37927,927,578

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18140841deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18140841Submitted genomicNC_000006.12:g.279
    58601_27959800del
    GRCh38 (hg38)NC_000006.12Chr627,958,60127,959,800
    nssv18140841RemappedPerfectNC_000006.11:g.279
    26379_27927578del
    GRCh37.p13First PassNC_000006.11Chr627,926,37927,927,578

    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)
    nssv18140841<0.001338924
    Support Center