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nsv6604620

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:40,384

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 266 SVs from 50 studies. See in: genome view    
    Submitted genomic23,496,556-23,536,939Question Mark
    Overlapping variant regions from other studies: 266 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):23,536,175-23,576,558Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6604620Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr723,496,55623,536,939
    nsv6604620RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr723,536,17523,576,558

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18154927deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18154927Submitted genomicNC_000007.14:g.234
    96556_23536939del
    GRCh38 (hg38)NC_000007.14Chr723,496,55623,536,939
    nssv18154927RemappedPerfectNC_000007.13:g.235
    36175_23576558del
    GRCh37.p13First PassNC_000007.13Chr723,536,17523,576,558

    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)
    nssv18154927<0.001139184
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