A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716269



Internal ID18667864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32102349..34034322hg38UCSC Ensembl
Innerchr16:32113670..33836789hg19UCSC Ensembl
Innerchr16:32021171..33744290hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381931974
hg191723120
hg181723120
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063161
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)nssv3716269
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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