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nsv6770190

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 93 SVs from 17 studies. See in: genome view    
    Submitted genomic73,545,001-73,551,600Question Mark
    Overlapping variant regions from other studies: 93 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):72,840,826-72,847,425Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6770190Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr573,545,00173,551,600
    nsv6770190RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr572,840,82672,847,425

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18705461duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18705461Submitted genomicNC_000005.10:g.735
    45001_73551600dup
    GRCh38 (hg38)NC_000005.10Chr573,545,00173,551,600
    nssv18705461RemappedPerfectNC_000005.9:g.7284
    0826_72847425dup
    GRCh37.p13First PassNC_000005.9Chr572,840,82672,847,425

    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)
    nssv187054614e-061274628
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