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nsv6564221

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:433

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 16 studies. See in: genome view    
    Submitted genomic149,506,465-149,506,897Question Mark
    Overlapping variant regions from other studies: 84 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):149,827,601-149,828,033Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6564221Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6149,506,465149,506,897
    nsv6564221RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6149,827,601149,828,033

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18269268inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18269268Submitted genomicNC_000006.12:g.149
    506465_149506897in
    v
    GRCh38 (hg38)NC_000006.12Chr6149,506,465149,506,897
    nssv18269268RemappedPerfectNC_000006.11:g.149
    827601_149828033in
    v
    GRCh37.p13First PassNC_000006.11Chr6149,827,601149,828,033

    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)
    nssv18269268<0.001336458
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