A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791746



Internal ID19159992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32593089..34034043hg38UCSC Ensembl
Innerchr16:32604410..33836510hg19UCSC Ensembl
Innerchr16:32511911..33744011hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381440955
hg191232101
hg181232101
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892840
Supporting Variants
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=275
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791746
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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