A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893673



Internal ID19184493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:23695630..23720880hg38UCSC Ensembl
Outerchr3:23695630..23720880hg38UCSC Ensembl
Innerchr3:23737121..23762371hg19UCSC Ensembl
Outerchr3:23737121..23762371hg19UCSC Ensembl
Innerchr3:23712125..23737375hg18UCSC Ensembl
Outerchr3:23712125..23737375hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3825251
hg1925251
hg1825251
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787756
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893673
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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