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nsv6737250

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,942

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 470 SVs from 52 studies. See in: genome view    
    Submitted genomic1,239,705-1,265,646Question Mark
    Overlapping variant regions from other studies: 470 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):1,233,493-1,259,434Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6737250Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr41,239,7051,265,646
    nsv6737250RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr41,233,4931,259,434

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18683274duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18683274Submitted genomicNC_000004.12:g.123
    9705_1265646dup
    GRCh38 (hg38)NC_000004.12Chr41,239,7051,265,646
    nssv18683274RemappedPerfectNC_000004.11:g.123
    3493_1259434dup
    GRCh37.p13First PassNC_000004.11Chr41,233,4931,259,434

    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)
    nssv186832747e-062274300
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