A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796112



Internal ID19163622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20535562..20557521hg38UCSC Ensembl
Innerchr16:20546884..20568843hg19UCSC Ensembl
Innerchr16:20454385..20476344hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3821960
hg1921960
hg1821960
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892808
Supporting Variants
Samples
Known GenesACSM2B
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796112
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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