A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891725



Internal ID18839435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33412332..33479056hg38UCSC Ensembl
Outerchr2:33412332..33479056hg38UCSC Ensembl
Innerchr2:33637399..33704123hg19UCSC Ensembl
Outerchr2:33637399..33704123hg19UCSC Ensembl
Innerchr2:33490903..33557627hg18UCSC Ensembl
Outerchr2:33490903..33557627hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3866725
hg1966725
hg1866725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789105
Samples
Known GenesRASGRP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891725
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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