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nsv7049533

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,301,501

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5203 SVs from 109 studies. See in: genome view    
    Submitted genomic244,971,072-246,272,572Question Mark
    Overlapping variant regions from other studies: 5206 SVs from 109 studies. See in: genome view    
    Remapped(Score: Perfect):245,134,374-246,435,874Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7049533Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1244,971,072246,272,572
    nsv7049533RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1245,134,374246,435,874

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759458inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759458Submitted genomicNC_000001.11:g.244
    971072_246272572in
    v
    GRCh38 (hg38)NC_000001.11Chr1244,971,072246,272,572
    nssv18759458RemappedPerfectNC_000001.10:g.245
    134374_246435874in
    v
    GRCh37.p13First PassNC_000001.10Chr1245,134,374246,435,874

    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)
    nssv187594584e-061276268
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