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nsv7040350

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75,159

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 280 SVs from 47 studies. See in: genome view    
    Submitted genomic228,097,467-228,172,625Question Mark
    Overlapping variant regions from other studies: 283 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):228,285,168-228,360,326Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040350Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1228,097,467228,172,625
    nsv7040350RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1228,285,168228,360,326

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761252inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761252Submitted genomicNC_000001.11:g.228
    097467_228172625in
    v
    GRCh38 (hg38)NC_000001.11Chr1228,097,467228,172,625
    nssv18761252RemappedPerfectNC_000001.10:g.228
    285168_228360326in
    v
    GRCh37.p13First PassNC_000001.10Chr1228,285,168228,360,326

    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)
    nssv187612524e-061276268
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