A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065801



Internal ID19155020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32147274..32944737hg38UCSC Ensembl
Innerchr16:32158595..32956058hg19UCSC Ensembl
Innerchr16:32066096..32863559hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38797464
hg19797464
hg18797464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2854n100
Supporting Variantsnssv3550343
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)nsv1065801
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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