A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625908



Internal ID7012742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34199171..34204543hg38UCSC Ensembl
Innerchr11:34199171..34204543hg38UCSC Ensembl
Outerchr11:34198964..34204818hg38UCSC Ensembl
chr11:34220718..34226090hg19UCSC Ensembl
Innerchr11:34220718..34226090hg19UCSC Ensembl
Outerchr11:34220511..34226365hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg385373
hg195373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14088615, essv14088616, essv14088614, essv14088617, essv14088613
SamplesNA18947, NA18565, NA18980, NA18561, NA18538
Known GenesABTB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625908
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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