A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787821



Internal ID19173411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:83013582..83088536hg38UCSC Ensembl
Innerchr17:80971458..81046412hg19UCSC Ensembl
Innerchr17:78564747..78639701hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3874955
hg1974955
hg1874955
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893053
Supporting Variants
Samples
Known GenesB3GNTL1, METRNL
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=21
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787821
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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