A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626062



Internal ID7012896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40401348..40592951hg38UCSC Ensembl
chr11:40422898..40614501hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38191604
hg19191604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14103226
SamplesNA20758
Known GenesLRRC4C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626062
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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