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nsv7076952

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,446

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 300 SVs from 58 studies. See in: genome view    
    Submitted genomic49,790,448-49,829,893Question Mark
    Overlapping variant regions from other studies: 294 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):49,812,000-49,851,445Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076952Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1149,790,44849,829,893
    nsv7076952RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1149,812,00049,851,445

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18739749inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18739749Submitted genomicNC_000011.10:g.497
    90448_49829893inv
    GRCh38 (hg38)NC_000011.10Chr1149,790,44849,829,893
    nssv18739749RemappedPerfectNC_000011.9:g.4981
    2000_49851445inv
    GRCh37.p13First PassNC_000011.9Chr1149,812,00049,851,445

    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)
    nssv187397497e-062274708
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