A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061556



Internal ID18804087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32022053..34032840hg38UCSC Ensembl
Innerchr16:32033374..33835307hg19UCSC Ensembl
Innerchr16:31940875..33742808hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382010788
hg191801934
hg181801934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3549257
Samples
Known GenesHERC2P4, LOC390705, 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)nsv1061556
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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