A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6045813



Internal ID9686012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:114938019..114949575hg38UCSC Ensembl
Outerchr3:114937398..114949945hg38UCSC Ensembl
Innerchr3:114656866..114668422hg19UCSC Ensembl
Outerchr3:114656245..114668792hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3812548
hg1912548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659892
Supporting Variants
SamplesNA19437
Known GenesZBTB20
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6045813
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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