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nsv6340329

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:40,567

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 174 SVs from 28 studies. See in: genome view    
    Submitted genomic49,866,938-49,907,504Question Mark
    Overlapping variant regions from other studies: 174 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):50,094,076-50,134,642Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6340329Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr249,866,93849,907,504
    nsv6340329RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr250,094,07650,134,642

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18086477deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18086477Submitted genomicNC_000002.12:g.498
    66938_49907504del
    GRCh38 (hg38)NC_000002.12Chr249,866,93849,907,504
    nssv18086477RemappedPerfectNC_000002.11:g.500
    94076_50134642del
    GRCh37.p13First PassNC_000002.11Chr250,094,07650,134,642

    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)
    nssv18086477<0.001139230
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