A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716273



Internal ID18667868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32135553..33813659hg38UCSC Ensembl
Innerchr16:32146874..33616126hg19UCSC Ensembl
Innerchr16:32054375..33523627hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381678107
hg191469253
hg181469253
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059179
Supporting Variants
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)nssv3716273
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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