A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891760



Internal ID19186156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:33981943..34138882hg38UCSC Ensembl
Outerchr2:33981943..34138882hg38UCSC Ensembl
Innerchr2:34207010..34363949hg19UCSC Ensembl
Outerchr2:34207010..34363949hg19UCSC Ensembl
Innerchr2:34060514..34217453hg18UCSC Ensembl
Outerchr2:34060514..34217453hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38156940
hg19156940
hg18156940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786592
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891760
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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