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nsv6928277

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:910

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 29 studies. See in: genome view    
    Submitted genomic9,923,391-9,924,300Question Mark
    Overlapping variant regions from other studies: 138 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):10,075,990-10,076,899Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6928277Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr129,923,3919,924,300
    nsv6928277RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,075,99010,076,899

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18374408deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18374408Submitted genomicNC_000012.12:g.992
    3391_9924300del
    GRCh38 (hg38)NC_000012.12Chr129,923,3919,924,300
    nssv18374408RemappedPerfectNC_000012.11:g.100
    75990_10076899del
    GRCh37.p13First PassNC_000012.11Chr1210,075,99010,076,899

    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)
    nssv183744080.002520270894
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