A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064716



Internal ID18807247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..33952512hg38UCSC Ensembl
Innerchr16:32180774..33754979hg19UCSC Ensembl
Innerchr16:32088275..33662480hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381783060
hg191574206
hg181574206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3550387, nssv3716304, nssv3716303
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)nsv1064716
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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