A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716221



Internal ID18667816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32022053..34056597hg38UCSC Ensembl
Innerchr16:32033374..33859064hg19UCSC Ensembl
Innerchr16:31940875..33766565hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382034545
hg191825691
hg181825691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058300
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)nssv3716221
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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