A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893524



Internal ID19184344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:193119895..194065682hg38UCSC Ensembl
Outerchr2:193119895..194065682hg38UCSC Ensembl
Innerchr2:193984621..194930406hg19UCSC Ensembl
Outerchr2:193984621..194930406hg19UCSC Ensembl
Innerchr2:193692866..194638651hg18UCSC Ensembl
Outerchr2:193692866..194638651hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38945788
hg19945786
hg18945786
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789140
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893524
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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