A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550344



Internal ID18848625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32147274..33002529hg38UCSC Ensembl
Innerchr16:32158595..33013850hg19UCSC Ensembl
Innerchr16:32066096..32921351hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38855256
hg19855256
hg18855256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057931
Supporting Variants
Samples
Known GenesHERC2P4, LOC390705, 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)nssv3550344
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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