U.S. flag

An official website of the United States government

nsv6900514

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,232

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 169 SVs from 42 studies. See in: genome view    
    Submitted genomic56,793,553-56,826,784Question Mark
    Overlapping variant regions from other studies: 171 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):56,561,029-56,594,260Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6900514Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1156,793,55356,826,784
    nsv6900514RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1156,561,02956,594,260

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351717deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351717Submitted genomicNC_000011.10:g.567
    93553_56826784del
    GRCh38 (hg38)NC_000011.10Chr1156,793,55356,826,784
    nssv18351717RemappedPerfectNC_000011.9:g.5656
    1029_56594260del
    GRCh37.p13First PassNC_000011.9Chr1156,561,02956,594,260

    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)
    nssv183517176e-051275688
    Support Center