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nsv7055294

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,874

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 139 SVs from 33 studies. See in: genome view    
    Submitted genomic110,528,628-110,535,501Question Mark
    Overlapping variant regions from other studies: 139 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):111,449,784-111,456,657Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055294Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4110,528,628110,535,501
    nsv7055294RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4111,449,784111,456,657

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772468inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772468Submitted genomicNC_000004.12:g.110
    528628_110535501in
    v
    GRCh38 (hg38)NC_000004.12Chr4110,528,628110,535,501
    nssv18772468RemappedPerfectNC_000004.11:g.111
    449784_111456657in
    v
    GRCh37.p13First PassNC_000004.11Chr4111,449,784111,456,657

    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)
    nssv187724684e-061276268
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