A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065657



Internal ID19154876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32217659..33908301hg38UCSC Ensembl
Innerchr16:32228980..33710768hg19UCSC Ensembl
Innerchr16:32136481..33618269hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381690643
hg191481789
hg181481789
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3716327, nssv3550457, nssv3550456, nssv3550458, nssv3716328, nssv3550455
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)nsv1065657
Frequency
Sample Size11257
Observed Gain2
Observed Loss4
Observed Complex0
Frequencyn/a


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