U.S. flag

An official website of the United States government

nsv6832629

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,972

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 81 SVs from 21 studies. See in: genome view    
    Submitted genomic43,285,602-43,289,573Question Mark
    Overlapping variant regions from other studies: 81 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):43,325,201-43,329,172Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6832629Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr743,285,60243,289,573
    nsv6832629RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr743,325,20143,329,172

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18542333deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18542333Submitted genomicNC_000007.14:g.432
    85602_43289573del
    GRCh38 (hg38)NC_000007.14Chr743,285,60243,289,573
    nssv18542333RemappedPerfectNC_000007.13:g.433
    25201_43329172del
    GRCh37.p13First PassNC_000007.13Chr743,325,20143,329,172

    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)
    nssv185423334e-061276146
    Support Center