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nsv6835475

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,744

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 28 studies. See in: genome view    
    Submitted genomic149,077,582-149,079,325Question Mark
    Overlapping variant regions from other studies: 165 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):148,774,674-148,776,417Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6835475Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7149,077,582149,079,325
    nsv6835475RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7148,774,674148,776,417

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18537242deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18537242Submitted genomicNC_000007.14:g.149
    077582_149079325de
    l
    GRCh38 (hg38)NC_000007.14Chr7149,077,582149,079,325
    nssv18537242RemappedPerfectNC_000007.13:g.148
    774674_148776417de
    l
    GRCh37.p13First PassNC_000007.13Chr7148,774,674148,776,417

    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)
    nssv18537242<0.00132254530
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