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nsv6922310

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:236

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 87 SVs from 28 studies. See in: genome view    
    Submitted genomic102,926,816-102,927,051Question Mark
    Overlapping variant regions from other studies: 87 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):103,320,594-103,320,829Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6922310Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12102,926,816102,927,051
    nsv6922310RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12103,320,594103,320,829

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18355521deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18355521Submitted genomicNC_000012.12:g.102
    926816_102927051de
    l
    GRCh38 (hg38)NC_000012.12Chr12102,926,816102,927,051
    nssv18355521RemappedPerfectNC_000012.11:g.103
    320594_103320829de
    l
    GRCh37.p13First PassNC_000012.11Chr12103,320,594103,320,829

    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)
    nssv183555210.0174024254182
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