A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669809



Internal ID9935914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73203051..73203990hg38UCSC Ensembl
chr11:72914096..72915035hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6278946, essv5625871, essv6153164, essv5558019, essv5416101, essv5683151, essv5495502, essv6185845, essv5684542, essv6086529, essv6245678, essv6125299, essv6567922, essv6591166, essv6583034, essv6542148, essv5491036
SamplesNA19377, NA19379, NA18874, NA20340, HG01440, NA18867, NA19347, NA18523, NA19108, NA19835, NA19311, NA19818, NA19398, NA18501, NA19116, NA19213, NA19312
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669809
Frequency
Sample Size1151
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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