A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716187



Internal ID18667782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31960187..33829351hg38UCSC Ensembl
Innerchr16:31971508..33631818hg19UCSC Ensembl
Innerchr16:31879009..33539319hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381869165
hg191660311
hg181660311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062421
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)nssv3716187
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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