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nsv7005768

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,323

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 260 SVs from 50 studies. See in: genome view    
    Submitted genomic11,808,748-11,848,070Question Mark
    Overlapping variant regions from other studies: 260 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):11,919,563-11,958,885Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7005768Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1911,808,74811,848,070
    nsv7005768RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1911,919,56311,958,885

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18638547duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18638547Submitted genomicNC_000019.10:g.118
    08748_11848070dup
    GRCh38 (hg38)NC_000019.10Chr1911,808,74811,848,070
    nssv18638547RemappedPerfectNC_000019.9:g.1191
    9563_11958885dup
    GRCh37.p13First PassNC_000019.9Chr1911,919,56311,958,885

    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)
    nssv186385476.7e-0519275598
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