A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893585



Internal ID18837719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63289..223742hg38UCSC Ensembl
Outerchr3:44574..267680hg38UCSC Ensembl
Innerchr3:104972..265425hg19UCSC Ensembl
Outerchr3:86256..309363hg19UCSC Ensembl
Innerchr3:79972..240425hg18UCSC Ensembl
Outerchr3:61256..284363hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38223107
hg19223108
hg18223108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787792, essv25791674
Samples
Known GenesCHL1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893585
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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