A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522906



Internal ID15103513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33670403..33679874hg38UCSC Ensembl
Innerchr6:33638180..33647651hg19UCSC Ensembl
Innerchr6:33746158..33755629hg18UCSC Ensembl
Innerchr6:33746158..33755629hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg389472
hg199472
hg189472
hg179472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698564
Samples
Known GenesITPR3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522906
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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