A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891826



Internal ID19186222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34570988..35202474hg38UCSC Ensembl
Outerchr2:34570988..35202474hg38UCSC Ensembl
Innerchr2:34796055..35427540hg19UCSC Ensembl
Outerchr2:34796055..35427540hg19UCSC Ensembl
Innerchr2:34649559..35281044hg18UCSC Ensembl
Outerchr2:34649559..35281044hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38631487
hg19631486
hg18631486
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788444
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891826
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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