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nsv7076860

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:92,156

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 742 SVs from 68 studies. See in: genome view    
    Submitted genomic152,453,419-152,545,574Question Mark
    Overlapping variant regions from other studies: 742 SVs from 68 studies. See in: genome view    
    Remapped(Score: Perfect):152,150,504-152,242,659Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076860Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7152,453,419152,545,574
    nsv7076860RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7152,150,504152,242,659

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782145inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782145Submitted genomicNC_000007.14:g.152
    453419_152545574in
    v
    GRCh38 (hg38)NC_000007.14Chr7152,453,419152,545,574
    nssv18782145RemappedPerfectNC_000007.13:g.152
    150504_152242659in
    v
    GRCh37.p13First PassNC_000007.13Chr7152,150,504152,242,659

    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)
    nssv187821455e-0514272198
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