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nsv7061790

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,905,475

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 19162 SVs from 120 studies. See in: genome view    
    Submitted genomic76,348,646-84,254,120Question Mark
    Overlapping variant regions from other studies: 19163 SVs from 120 studies. See in: genome view    
    Remapped(Score: Perfect):76,922,782-84,828,255Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061790Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1376,348,64684,254,120
    nsv7061790RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1376,922,78284,828,255

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753841inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753841Submitted genomicNC_000013.11:g.763
    48646_84254120inv
    GRCh38 (hg38)NC_000013.11Chr1376,348,64684,254,120
    nssv18753841RemappedPerfectNC_000013.10:g.769
    22782_84828255inv
    GRCh37.p13First PassNC_000013.10Chr1376,922,78284,828,255

    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)
    nssv187538417e-062276160
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