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nsv6607316

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 34 studies. See in: genome view    
    Submitted genomic99,593,201-99,598,000Question Mark
    Overlapping variant regions from other studies: 125 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):99,190,824-99,195,623Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6607316Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr799,593,20199,598,000
    nsv6607316RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr799,190,82499,195,623

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18162438deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18162438Submitted genomicNC_000007.14:g.995
    93201_99598000del
    GRCh38 (hg38)NC_000007.14Chr799,593,20199,598,000
    nssv18162438RemappedPerfectNC_000007.13:g.991
    90824_99195623del
    GRCh37.p13First PassNC_000007.13Chr799,190,82499,195,623

    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)
    nssv18162438<0.001237438
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