A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893635



Internal ID18837769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3985921..4124049hg38UCSC Ensembl
Outerchr3:3899706..4211535hg38UCSC Ensembl
Innerchr3:4027605..4165733hg19UCSC Ensembl
Outerchr3:3941390..4253219hg19UCSC Ensembl
Innerchr3:4002605..4140733hg18UCSC Ensembl
Outerchr3:3916390..4228219hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38311830
hg19311830
hg18311830
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779486, essv25799326
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893635
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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