A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6505472



Internal ID9438339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73709104..73715882hg38UCSC Ensembl
chr11:73420149..73426927hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg386779
hg196779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665533
Supporting Variants
SamplesNA18637
Known GenesRAB6A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6505472
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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