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nsv6378672

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,647

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 130 SVs from 29 studies. See in: genome view    
    Submitted genomic73,492,466-73,500,112Question Mark
    Overlapping variant regions from other studies: 130 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):74,358,183-74,365,829Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6378672Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr473,492,46673,500,112
    nsv6378672RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr474,358,18374,365,829

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18120905deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18120905Submitted genomicNC_000004.12:g.734
    92466_73500112del
    GRCh38 (hg38)NC_000004.12Chr473,492,46673,500,112
    nssv18120905RemappedPerfectNC_000004.11:g.743
    58183_74365829del
    GRCh37.p13First PassNC_000004.11Chr474,358,18374,365,829

    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)
    nssv18120905<0.001139196
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