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nsv7032924

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,903,154

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8928 SVs from 92 studies. See in: genome view    
    Submitted genomic34,355,734-41,258,887Question Mark
    Overlapping variant regions from other studies: 8895 SVs from 92 studies. See in: genome view    
    Remapped(Score: Good):34,373,851-41,118,140Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7032924Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX34,355,73441,258,887
    nsv7032924RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX34,373,85141,118,140

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18764418inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18764418Submitted genomicNC_000023.11:g.343
    55734_41258887inv
    GRCh38 (hg38)NC_000023.11ChrX34,355,73441,258,887
    nssv18764418RemappedGoodNC_000023.10:g.343
    73851_41118140inv
    GRCh37.p13First PassNC_000023.10ChrX34,373,85141,118,140

    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)
    nssv187644185e-061200000
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