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nsv6732918

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:208,117

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 899 SVs from 76 studies. See in: genome view    
    Submitted genomic8,222,989-8,431,105Question Mark
    Overlapping variant regions from other studies: 899 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):8,224,716-8,432,832Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6732918Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr48,222,9898,431,105
    nsv6732918RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr48,224,7168,432,832

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18500185deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18500185Submitted genomicNC_000004.12:g.822
    2989_8431105del
    GRCh38 (hg38)NC_000004.12Chr48,222,9898,431,105
    nssv18500185RemappedPerfectNC_000004.11:g.822
    4716_8432832del
    GRCh37.p13First PassNC_000004.11Chr48,224,7168,432,832

    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)
    nssv185001857e-062276128
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