A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662605



Internal ID9928710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74050711..74051277hg38UCSC Ensembl
chr11:73761756..73762322hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5817809, essv5430039, essv6214061, essv6098883, essv6268775, essv5605579, essv6448022, essv6187526, essv6276477, essv5490335, essv5529973, essv6069832, essv6550613, essv5727244, essv6038755, essv5433704, essv5932015, essv5401525
SamplesNA19700, NA19909, NA18508, NA19920, NA19448, NA19138, NA18498, NA19239, NA19908, NA18853, NA20296, NA19108, NA19240, NA19311, NA18501, NA19713, NA19213, NA19312
Known GenesC2CD3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662605
Frequency
Sample Size1151
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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