A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796400



Internal ID19167561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:17337244..17436605hg38UCSC Ensembl
Innerchr21:18709563..18808923hg19UCSC Ensembl
Innerchr21:17631434..17730794hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3899362
hg1999361
hg1899361
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893380
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796400
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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