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nsv7039666

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:121

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 35 studies. See in: genome view    
    Submitted genomic205,884,453-205,884,573Question Mark
    Overlapping variant regions from other studies: 146 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):205,853,581-205,853,701Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039666Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1205,884,453205,884,573
    nsv7039666RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1205,853,581205,853,701

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18750764inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18750764Submitted genomicNC_000001.11:g.205
    884453_205884573in
    v
    GRCh38 (hg38)NC_000001.11Chr1205,884,453205,884,573
    nssv18750764RemappedPerfectNC_000001.10:g.205
    853581_205853701in
    v
    GRCh37.p13First PassNC_000001.10Chr1205,853,581205,853,701

    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)
    nssv18750764<0.00135266914
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