A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626658



Internal ID6666808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64289409..64294476hg38UCSC Ensembl
Innerchr11:64289426..64294459hg38UCSC Ensembl
Outerchr11:64289392..64294493hg38UCSC Ensembl
chr11:64056881..64061948hg19UCSC Ensembl
Innerchr11:64056898..64061931hg19UCSC Ensembl
Outerchr11:64056864..64061965hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385068
hg195068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14184927
SamplesNA19314
Known GenesGPR137, KCNK4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626658
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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