A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6004052



Internal ID9672682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108469066..108470770hg38UCSC Ensembl
chr11:108339793..108341497hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665383
Supporting Variants
SamplesNA19401
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6004052
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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