A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626887



Internal ID6667035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77586275..77593068hg38UCSC Ensembl
Innerchr11:77586275..77593068hg38UCSC Ensembl
Outerchr11:77585775..77593568hg38UCSC Ensembl
chr11:77297320..77304113hg19UCSC Ensembl
Innerchr11:77297320..77304113hg19UCSC Ensembl
Outerchr11:77296820..77304613hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg386794
hg196794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14214978
SamplesNA18567
Known GenesAQP11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626887
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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