A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065975



Internal ID18808506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32197413..34061880hg38UCSC Ensembl
Innerchr16:32208734..33864347hg19UCSC Ensembl
Innerchr16:32116235..33771848hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381864468
hg191655614
hg181655614
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3550415, nssv3550416
Samples
Known GenesLOC390705, 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)nsv1065975
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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