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nsv7065209

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 23 studies. See in: genome view    
    Submitted genomic130,450,591-130,450,632Question Mark
    Overlapping variant regions from other studies: 123 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):133,325,978-133,326,019Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065209Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9130,450,591130,450,632
    nsv7065209RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9133,325,978133,326,019

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785496inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785496Submitted genomicNC_000009.12:g.130
    450591_130450632in
    v
    GRCh38 (hg38)NC_000009.12Chr9130,450,591130,450,632
    nssv18785496RemappedPerfectNC_000009.11:g.133
    325978_133326019in
    v
    GRCh37.p13First PassNC_000009.11Chr9133,325,978133,326,019

    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)
    nssv187854964e-061276230
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