A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699465



Internal ID15089431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163437205..163486853hg38UCSC Ensembl
Innerchr6:163858237..163907885hg19UCSC Ensembl
Innerchr6:163778227..163827875hg18UCSC Ensembl
Innerchr6:163828648..163878296hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3849649
hg1949649
hg1849649
hg1749649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523664
Supporting Variants
Samples
Known GenesQKI
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699465
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer