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nsv6578359

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,855,698

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 23249 SVs from 129 studies. See in: genome view    
    Submitted genomic56,201,986-66,057,683Question Mark
    Overlapping variant regions from other studies: 23249 SVs from 129 studies. See in: genome view    
    Remapped(Score: Perfect):56,595,770-66,451,463Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6578359Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1256,201,98666,057,683
    nsv6578359RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1256,595,77066,451,463

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18229330inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18229330Submitted genomicNC_000012.12:g.562
    01986_66057683inv
    GRCh38 (hg38)NC_000012.12Chr1256,201,98666,057,683
    nssv18229330RemappedPerfectNC_000012.11:g.565
    95770_66451463inv
    GRCh37.p13First PassNC_000012.11Chr1256,595,77066,451,463

    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)
    nssv18229330<0.001436524
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