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nsv7073954

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:419,862

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1181 SVs from 74 studies. See in: genome view    
    Submitted genomic14,354,467-14,774,328Question Mark
    Overlapping variant regions from other studies: 1182 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):14,507,401-14,927,262Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073954Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1214,354,46714,774,328
    nsv7073954RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1214,507,40114,927,262

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752201inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752201Submitted genomicNC_000012.12:g.143
    54467_14774328inv
    GRCh38 (hg38)NC_000012.12Chr1214,354,46714,774,328
    nssv18752201RemappedPerfectNC_000012.11:g.145
    07401_14927262inv
    GRCh37.p13First PassNC_000012.11Chr1214,507,40114,927,262

    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)
    nssv187522017e-062276268
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