A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586033



Internal ID7057415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88831228..89222453hg38UCSC Ensembl
Innerchr2:89130741..89521934hg19UCSC Ensembl
Innerchr2:88911856..89303049hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38391226
hg19391194
hg18391194
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990340
Supporting Variants
SamplesHuRef
Known Genes
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586033
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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