A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064113



Internal ID19153332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32147274..33908301hg38UCSC Ensembl
Innerchr16:32158595..33710768hg19UCSC Ensembl
Innerchr16:32066096..33618269hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381761028
hg191552174
hg181552174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2842n100
Supporting Variantsnssv3550352
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)nsv1064113
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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