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nsv7006917

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,392

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 32 studies. See in: genome view    
    Submitted genomic48,808,493-48,819,884Question Mark
    Overlapping variant regions from other studies: 119 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):49,311,750-49,323,141Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7006917Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,808,49348,819,884
    nsv7006917RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,311,75049,323,141

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18640903duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18640903Submitted genomicNC_000019.10:g.488
    08493_48819884dup
    GRCh38 (hg38)NC_000019.10Chr1948,808,49348,819,884
    nssv18640903RemappedPerfectNC_000019.9:g.4931
    1750_49323141dup
    GRCh37.p13First PassNC_000019.9Chr1949,311,75049,323,141

    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)
    nssv186409031.8e-055275514
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