nsv6808371

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:111,527

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 570 SVs from 70 studies. See in: genome view    
    Submitted genomic17,385,230-17,496,756Question Mark
    Overlapping variant regions from other studies: 570 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):17,424,854-17,536,380Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6808371Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr717,385,23017,496,756
    nsv6808371RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr717,424,85417,536,380

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18538814deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18538814Submitted genomicNC_000007.14:g.173
    85230_17496756del
    GRCh38 (hg38)NC_000007.14Chr717,385,23017,496,756
    nssv18538814RemappedPerfectNC_000007.13:g.174
    24854_17536380del
    GRCh37.p13First PassNC_000007.13Chr717,424,85417,536,380

    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)
    nssv185388144e-061276134
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