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nsv6333744

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 153 SVs from 20 studies. See in: genome view    
    Submitted genomic173,476,801-173,477,500Question Mark
    Overlapping variant regions from other studies: 156 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):173,445,940-173,446,639Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6333744Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1173,476,801173,477,500
    nsv6333744RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1173,445,940173,446,639

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18053123deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18053123Submitted genomicNC_000001.11:g.173
    476801_173477500de
    l
    GRCh38 (hg38)NC_000001.11Chr1173,476,801173,477,500
    nssv18053123RemappedPerfectNC_000001.10:g.173
    445940_173446639de
    l
    GRCh37.p13First PassNC_000001.10Chr1173,445,940173,446,639

    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)
    nssv180531230.081309838086
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