A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520222



Internal ID15447515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32126644..34034043hg38UCSC Ensembl
Innerchr16:32137965..33836510hg19UCSC Ensembl
Innerchr16:32045466..33744011hg18UCSC Ensembl
Innerchr16:32045466..33744011hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381907400
hg191698546
hg181698546
hg171698546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697290
Samples
Known GenesHERC2P4, LOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520222
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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