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nsv6592543

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,235,336

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3175 SVs from 103 studies. See in: genome view    
    Submitted genomic74,064,999-75,300,334Question Mark
    Overlapping variant regions from other studies: 3176 SVs from 103 studies. See in: genome view    
    Remapped(Score: Perfect):74,357,340-75,592,675Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6592543Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1574,064,99975,300,334
    nsv6592543RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1574,357,34075,592,675

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18241925inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18241925Submitted genomicNC_000015.10:g.740
    64999_75300334inv
    GRCh38 (hg38)NC_000015.10Chr1574,064,99975,300,334
    nssv18241925RemappedPerfectNC_000015.9:g.7435
    7340_75592675inv
    GRCh37.p13First PassNC_000015.9Chr1574,357,34075,592,675

    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)
    nssv182419250.0023922420
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