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nsv6435227

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:421,789

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1537 SVs from 78 studies. See in: genome view    
    Submitted genomic146,629,505-147,051,293Question Mark
    Overlapping variant regions from other studies: 1537 SVs from 78 studies. See in: genome view    
    Remapped(Score: Perfect):146,326,597-146,748,385Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6435227Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7146,629,505147,051,293
    nsv6435227RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7146,326,597146,748,385

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18155861deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18155861Submitted genomicNC_000007.14:g.146
    629505_147051293de
    l
    GRCh38 (hg38)NC_000007.14Chr7146,629,505147,051,293
    nssv18155861RemappedPerfectNC_000007.13:g.146
    326597_146748385de
    l
    GRCh37.p13First PassNC_000007.13Chr7146,326,597146,748,385

    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)
    nssv18155861<0.001139232
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