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nsv6386313

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:550

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 21 studies. See in: genome view    
    Submitted genomic109,963,966-109,964,515Question Mark
    Overlapping variant regions from other studies: 95 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):110,885,122-110,885,671Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6386313Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4109,963,966109,964,515
    nsv6386313RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4110,885,122110,885,671

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18107786deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18107786Submitted genomicNC_000004.12:g.109
    963966_109964515de
    l
    GRCh38 (hg38)NC_000004.12Chr4109,963,966109,964,515
    nssv18107786RemappedPerfectNC_000004.11:g.110
    885122_110885671de
    l
    GRCh37.p13First PassNC_000004.11Chr4110,885,122110,885,671

    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)
    nssv18107786<0.0011038228
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