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nsv7002236

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,000

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 26 studies. See in: genome view    
    Submitted genomic5,692,001-5,695,000Question Mark
    Overlapping variant regions from other studies: 112 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):5,692,012-5,695,011Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7002236Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr195,692,0015,695,000
    nsv7002236RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr195,692,0125,695,011

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639692duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639692Submitted genomicNC_000019.10:g.569
    2001_5695000dup
    GRCh38 (hg38)NC_000019.10Chr195,692,0015,695,000
    nssv18639692RemappedPerfectNC_000019.9:g.5692
    012_5695011dup
    GRCh37.p13First PassNC_000019.9Chr195,692,0125,695,011

    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)
    nssv186396926e-061172166
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