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nsv7045408

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,304

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 42 studies. See in: genome view    
    Submitted genomic180,190,212-180,191,515Question Mark
    Overlapping variant regions from other studies: 145 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):179,617,212-179,618,515Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045408Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5180,190,212180,191,515
    nsv7045408RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5179,617,212179,618,515

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775920inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775920Submitted genomicNC_000005.10:g.180
    190212_180191515in
    v
    GRCh38 (hg38)NC_000005.10Chr5180,190,212180,191,515
    nssv18775920RemappedPerfectNC_000005.9:g.1796
    17212_179618515inv
    GRCh37.p13First PassNC_000005.9Chr5179,617,212179,618,515

    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)
    nssv18775920<0.00174267664
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