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nsv6608468

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:884

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 36 studies. See in: genome view    
    Submitted genomic56,034,988-56,035,871Question Mark
    Overlapping variant regions from other studies: 105 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):56,102,681-56,103,564Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6608468Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr756,034,98856,035,871
    nsv6608468RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr756,102,68156,103,564

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18234894duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18234894Submitted genomicNC_000007.14:g.560
    34988_56035871dup
    GRCh38 (hg38)NC_000007.14Chr756,034,98856,035,871
    nssv18234894RemappedPerfectNC_000007.13:g.561
    02681_56103564dup
    GRCh37.p13First PassNC_000007.13Chr756,102,68156,103,564

    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)
    nssv18234894<0.001238914
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