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nsv6604659

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:787

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 26 studies. See in: genome view    
    Submitted genomic99,591,437-99,592,223Question Mark
    Overlapping variant regions from other studies: 111 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):99,189,060-99,189,846Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6604659Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr799,591,43799,592,223
    nsv6604659RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr799,189,06099,189,846

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18162436deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18162436Submitted genomicNC_000007.14:g.995
    91437_99592223del
    GRCh38 (hg38)NC_000007.14Chr799,591,43799,592,223
    nssv18162436RemappedPerfectNC_000007.13:g.991
    89060_99189846del
    GRCh37.p13First PassNC_000007.13Chr799,189,06099,189,846

    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)
    nssv18162436<0.001132788
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