A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067549



Internal ID19156768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32481160..34061880hg38UCSC Ensembl
Innerchr16:32492481..33864347hg19UCSC Ensembl
Innerchr16:32399982..33771848hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381580721
hg191371867
hg181371867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2873n100
Supporting Variantsnssv3551787
Samples
Known GenesLOC390705, 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)nsv1067549
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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