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nsv6404787

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:588

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 23 studies. See in: genome view    
    Submitted genomic49,736,960-49,737,547Question Mark
    Overlapping variant regions from other studies: 105 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):49,704,673-49,705,260Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6404787Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr649,736,96049,737,547
    nsv6404787RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr649,704,67349,705,260

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18142822deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18142822Submitted genomicNC_000006.12:g.497
    36960_49737547del
    GRCh38 (hg38)NC_000006.12Chr649,736,96049,737,547
    nssv18142822RemappedPerfectNC_000006.11:g.497
    04673_49705260del
    GRCh37.p13First PassNC_000006.11Chr649,704,67349,705,260

    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)
    nssv18142822<0.0011537602
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