A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6037273



Internal ID9117664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33993274..33996500hg38UCSC Ensembl
chr11:34014821..34018047hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383227
hg193227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662833
Supporting Variants
SamplesHG01125
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6037273
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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