A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626061



Internal ID7012895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40400848..40432924hg38UCSC Ensembl
Innerchr11:40400848..40432924hg38UCSC Ensembl
Outerchr11:40400348..40433424hg38UCSC Ensembl
chr11:40422398..40454474hg19UCSC Ensembl
Innerchr11:40422398..40454474hg19UCSC Ensembl
Outerchr11:40421898..40454974hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3832077
hg1932077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14103225
SamplesNA20758
Known GenesLRRC4C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626061
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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