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nsv7044955

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:366,693

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 811 SVs from 71 studies. See in: genome view    
    Submitted genomic107,297,913-107,664,605Question Mark
    Overlapping variant regions from other studies: 812 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):107,840,535-108,207,227Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044955Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1107,297,913107,664,605
    nsv7044955RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1107,840,535108,207,227

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18739779inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18739779Submitted genomicNC_000001.11:g.107
    297913_107664605in
    v
    GRCh38 (hg38)NC_000001.11Chr1107,297,913107,664,605
    nssv18739779RemappedPerfectNC_000001.10:g.107
    840535_108207227in
    v
    GRCh37.p13First PassNC_000001.10Chr1107,840,535108,207,227

    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)
    nssv187397794e-061276268
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