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nsv6665645

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,054

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 25 studies. See in: genome view    
    Submitted genomic47,893,852-47,896,905Question Mark
    Overlapping variant regions from other studies: 144 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):48,120,991-48,124,044Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6665645Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr247,893,85247,896,905
    nsv6665645RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr248,120,99148,124,044

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18465642deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18465642Submitted genomicNC_000002.12:g.478
    93852_47896905del
    GRCh38 (hg38)NC_000002.12Chr247,893,85247,896,905
    nssv18465642RemappedPerfectNC_000002.11:g.481
    20991_48124044del
    GRCh37.p13First PassNC_000002.11Chr248,120,99148,124,044

    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)
    nssv184656427e-062275908
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