A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791674



Internal ID18826353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44574..267680hg38UCSC Ensembl
Innerchr3:86256..309363hg19UCSC Ensembl
Innerchr3:61256..284363hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38223107
hg19223108
hg18223108
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 HumanHap 610
CommentsNumber of probes=100
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791674
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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