A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798702



Internal ID18833206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46755299..46809120hg38UCSC Ensembl
Innerchr3:46796789..46850610hg19UCSC Ensembl
Innerchr3:46771793..46825614hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3853822
hg1953822
hg1853822
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893692
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798702
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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