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nsv6638542

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:153

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 142 SVs from 29 studies. See in: genome view    
    Submitted genomic101,972,159-101,972,311Question Mark
    Overlapping variant regions from other studies: 142 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):102,437,715-102,437,867Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6638542Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1101,972,159101,972,311
    nsv6638542RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1102,437,715102,437,867

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18590856duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18590856Submitted genomicNC_000001.11:g.101
    972159_101972311du
    p
    GRCh38 (hg38)NC_000001.11Chr1101,972,159101,972,311
    nssv18590856RemappedPerfectNC_000001.10:g.102
    437715_102437867du
    p
    GRCh37.p13First PassNC_000001.10Chr1102,437,715102,437,867

    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)
    nssv185908561.3e-053230268
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