A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788232



Internal ID18817859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15950943..16030711hg38UCSC Ensembl
Innerchr17:15854257..15934025hg19UCSC Ensembl
Innerchr17:15794982..15874750hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3879769
hg1979769
hg1879769
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892973
Supporting Variants
Samples
Known GenesADORA2B, NCOR1, TTC19, ZSWIM7
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788232
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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