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nsv6325277

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,473

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 26 studies. See in: genome view    
    Submitted genomic150,699,524-150,702,996Question Mark
    Overlapping variant regions from other studies: 125 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):150,672,000-150,675,472Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6325277Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1150,699,524150,702,996
    nsv6325277RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1150,672,000150,675,472

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18052985deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18052985Submitted genomicNC_000001.11:g.150
    699524_150702996de
    l
    GRCh38 (hg38)NC_000001.11Chr1150,699,524150,702,996
    nssv18052985RemappedPerfectNC_000001.10:g.150
    672000_150675472de
    l
    GRCh37.p13First PassNC_000001.10Chr1150,672,000150,675,472

    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)
    nssv18052985<0.001639190
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