A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056990



Internal ID18799521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32047162..33002529hg38UCSC Ensembl
Innerchr16:32058483..33013850hg19UCSC Ensembl
Innerchr16:31965984..32921351hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38955368
hg19955368
hg18955368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2838n100
Supporting Variantsnssv3549265
Samples
Known GenesHERC2P4, LOC390705, 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)nsv1056990
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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