A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064762



Internal ID19153981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32217659..34009022hg38UCSC Ensembl
Innerchr16:32228980..33811489hg19UCSC Ensembl
Innerchr16:32136481..33718990hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381791364
hg191582510
hg181582510
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3550475, nssv3550474, nssv3550477, nssv3550476
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)nsv1064762
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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