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nsv7005690

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,944

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 279 SVs from 51 studies. See in: genome view    
    Submitted genomic2,276,293-2,308,236Question Mark
    Overlapping variant regions from other studies: 279 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):2,276,292-2,308,235Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7005690Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr192,276,2932,308,236
    nsv7005690RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr192,276,2922,308,235

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18421746deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18421746Submitted genomicNC_000019.10:g.227
    6293_2308236del
    GRCh38 (hg38)NC_000019.10Chr192,276,2932,308,236
    nssv18421746RemappedPerfectNC_000019.9:g.2276
    292_2308235del
    GRCh37.p13First PassNC_000019.9Chr192,276,2922,308,235

    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)
    nssv184217464e-061276214
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