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nsv6373822

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,991

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 160 SVs from 47 studies. See in: genome view    
    Submitted genomic154,374,344-154,379,334Question Mark
    Overlapping variant regions from other studies: 160 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):154,092,133-154,097,123Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6373822Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3154,374,344154,379,334
    nsv6373822RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3154,092,133154,097,123

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18096152deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18096152Submitted genomicNC_000003.12:g.154
    374344_154379334de
    l
    GRCh38 (hg38)NC_000003.12Chr3154,374,344154,379,334
    nssv18096152RemappedPerfectNC_000003.11:g.154
    092133_154097123de
    l
    GRCh37.p13First PassNC_000003.11Chr3154,092,133154,097,123

    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)
    nssv18096152<0.001239088
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