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nsv6785085

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70,106

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 247 SVs from 43 studies. See in: genome view    
    Submitted genomic49,671,798-49,741,903Question Mark
    Overlapping variant regions from other studies: 247 SVs from 43 studies. See in: genome view    
    Remapped(Score: Perfect):49,639,511-49,709,616Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6785085Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr649,671,79849,741,903
    nsv6785085RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr649,639,51149,709,616

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18528123deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18528123Submitted genomicNC_000006.12:g.496
    71798_49741903del
    GRCh38 (hg38)NC_000006.12Chr649,671,79849,741,903
    nssv18528123RemappedPerfectNC_000006.11:g.496
    39511_49709616del
    GRCh37.p13First PassNC_000006.11Chr649,639,51149,709,616

    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)
    nssv185281234e-061276130
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