A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664722



Internal ID9930827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3746250..3746894hg38UCSC Ensembl
chr11:3767480..3768124hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5848407, essv6249358, essv5565513, essv5782466, essv6495879, essv5437342, essv6134658
SamplesNA19397, HG01052, NA19332, NA19396, HG01124, NA19473, NA19334
Known GenesNUP98
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664722
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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