A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657626



Internal ID9923731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41807252..41807548hg38UCSC Ensembl
Outerchr11:41807215..41807598hg38UCSC Ensembl
Innerchr11:41828802..41829098hg19UCSC Ensembl
Outerchr11:41828765..41829148hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6339826
SamplesNA18595
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657626
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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