U.S. flag

An official website of the United States government

nsv6607544

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:506

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 29 studies. See in: genome view    
    Submitted genomic99,587,483-99,587,988Question Mark
    Overlapping variant regions from other studies: 115 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):99,185,106-99,185,611Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6607544Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr799,587,48399,587,988
    nsv6607544RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr799,185,10699,185,611

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18162434deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18162434Submitted genomicNC_000007.14:g.995
    87483_99587988del
    GRCh38 (hg38)NC_000007.14Chr799,587,48399,587,988
    nssv18162434RemappedPerfectNC_000007.13:g.991
    85106_99185611del
    GRCh37.p13First PassNC_000007.13Chr799,185,10699,185,611

    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)
    nssv18162434<0.001129890
    Support Center