A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779486



Internal ID18816802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3985921..4211535hg38UCSC Ensembl
Innerchr3:4027605..4253219hg19UCSC Ensembl
Innerchr3:4002605..4228219hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38225615
hg19225615
hg18225615
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893635
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=77
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779486
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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