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nsv7072662

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,302

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 164 SVs from 39 studies. See in: genome view    
    Submitted genomic52,646,395-52,649,696Question Mark
    Overlapping variant regions from other studies: 164 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):53,149,648-53,152,949Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072662Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1952,646,39552,649,696
    nsv7072662RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1953,149,64853,152,949

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760671inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760671Submitted genomicNC_000019.10:g.526
    46395_52649696inv
    GRCh38 (hg38)NC_000019.10Chr1952,646,39552,649,696
    nssv18760671RemappedPerfectNC_000019.9:g.5314
    9648_53152949inv
    GRCh37.p13First PassNC_000019.9Chr1953,149,64853,152,949

    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)
    nssv18760671<0.00159274052
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