A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5534464



Internal ID9505289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39695176..39697381hg38UCSC Ensembl
chr11:39716726..39718931hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382206
hg192206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676979
Supporting Variants
SamplesNA18985
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5534464
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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