A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891948



Internal ID19186344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41064119..41266259hg38UCSC Ensembl
Outerchr2:41064119..41266259hg38UCSC Ensembl
Innerchr2:41291259..41493399hg19UCSC Ensembl
Outerchr2:41291259..41493399hg19UCSC Ensembl
Innerchr2:41144763..41346903hg18UCSC Ensembl
Outerchr2:41144763..41346903hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38202141
hg19202141
hg18202141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778917
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891948
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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