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nsv6753945

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:110

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 242 SVs from 30 studies. See in: genome view    
    Submitted genomic184,188,626-184,188,735Question Mark
    Overlapping variant regions from other studies: 242 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):185,109,779-185,109,888Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6753945Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4184,188,626184,188,735
    nsv6753945RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4185,109,779185,109,888

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18493123deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18493123Submitted genomicNC_000004.12:g.184
    188626_184188735de
    l
    GRCh38 (hg38)NC_000004.12Chr4184,188,626184,188,735
    nssv18493123RemappedPerfectNC_000004.11:g.185
    109779_185109888de
    l
    GRCh37.p13First PassNC_000004.11Chr4185,109,779185,109,888

    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)
    nssv184931237.3e-0518242238
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