A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892592



Internal ID19183412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:67724729..67803187hg38UCSC Ensembl
Outerchr2:67724729..67803187hg38UCSC Ensembl
Innerchr2:67951861..68030319hg19UCSC Ensembl
Outerchr2:67951861..68030319hg19UCSC Ensembl
Innerchr2:67805365..67883823hg18UCSC Ensembl
Outerchr2:67805365..67883823hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3878459
hg1978459
hg1878459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798080
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892592
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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