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nsv6381077

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:108,010

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 369 SVs from 39 studies. See in: genome view    
    Submitted genomic70,714,621-70,822,630Question Mark
    Overlapping variant regions from other studies: 369 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):71,580,338-71,688,347Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6381077Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr470,714,62170,822,630
    nsv6381077RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr471,580,33871,688,347

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18211724duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18211724Submitted genomicNC_000004.12:g.707
    14621_70822630dup
    GRCh38 (hg38)NC_000004.12Chr470,714,62170,822,630
    nssv18211724RemappedPerfectNC_000004.11:g.715
    80338_71688347dup
    GRCh37.p13First PassNC_000004.11Chr471,580,33871,688,347

    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)
    nssv18211724<0.001139274
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