A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891971



Internal ID19186367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41557765..41658633hg38UCSC Ensembl
Outerchr2:41557765..41658633hg38UCSC Ensembl
Innerchr2:41784905..41885773hg19UCSC Ensembl
Outerchr2:41784905..41885773hg19UCSC Ensembl
Innerchr2:41638409..41739277hg18UCSC Ensembl
Outerchr2:41638409..41739277hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38100869
hg19100869
hg18100869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797180
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891971
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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