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nsv6742177

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55,653

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 324 SVs from 46 studies. See in: genome view    
    Submitted genomic177,308,317-177,363,969Question Mark
    Overlapping variant regions from other studies: 324 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):178,229,471-178,285,123Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6742177Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4177,308,317177,363,969
    nsv6742177RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4178,229,471178,285,123

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18495672deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18495672Submitted genomicNC_000004.12:g.177
    308317_177363969de
    l
    GRCh38 (hg38)NC_000004.12Chr4177,308,317177,363,969
    nssv18495672RemappedPerfectNC_000004.11:g.178
    229471_178285123de
    l
    GRCh37.p13First PassNC_000004.11Chr4178,229,471178,285,123

    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)
    nssv184956724e-061276162
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