A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674695



Internal ID9940800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34239588..34240936hg38UCSC Ensembl
Outerchr11:34239551..34240986hg38UCSC Ensembl
Innerchr11:34261135..34262483hg19UCSC Ensembl
Outerchr11:34261098..34262533hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381436
hg191436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6150287
SamplesNA19440
Known GenesABTB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674695
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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