A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760882



Internal ID18735128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:81547086..81550048hg38UCSC Ensembl
Outerchr3:81546293..81550576hg38UCSC Ensembl
Innerchr3:81596237..81599199hg19UCSC Ensembl
Outerchr3:81595444..81599727hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg384284
hg194284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562135
Supporting Variants
Samples
Known GenesGBE1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760882
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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