A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787792



Internal ID18834399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63289..223742hg38UCSC Ensembl
Innerchr3:104972..265425hg19UCSC Ensembl
Innerchr3:79972..240425hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38160454
hg19160454
hg18160454
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893585
Supporting Variants
Samples
Known GenesCHL1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=46
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787792
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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