A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065441



Internal ID18807972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32269023..34208804hg38UCSC Ensembl
Innerchr16:32280344..34011271hg19UCSC Ensembl
Innerchr16:32187845..33918772hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381939782
hg191730928
hg181730928
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3550593
Samples
Known GenesLINC00273, LOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065441
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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