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nsv7070987

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,176

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 122 SVs from 24 studies. See in: genome view    
    Submitted genomic65,545,353-65,550,528Question Mark
    Overlapping variant regions from other studies: 122 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):66,457,588-66,462,763Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070987Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr865,545,35365,550,528
    nsv7070987RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr866,457,58866,462,763

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783552inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783552Submitted genomicNC_000008.11:g.655
    45353_65550528inv
    GRCh38 (hg38)NC_000008.11Chr865,545,35365,550,528
    nssv18783552RemappedPerfectNC_000008.10:g.664
    57588_66462763inv
    GRCh37.p13First PassNC_000008.10Chr866,457,58866,462,763

    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)
    nssv187835524e-061276268
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