A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716296



Internal ID18667891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32135553..34061880hg38UCSC Ensembl
Innerchr16:32146874..33864347hg19UCSC Ensembl
Innerchr16:32054375..33771848hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381926328
hg191717474
hg181717474
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055482
Supporting Variants
Samples
Known GenesHERC2P4, LOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3716296
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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