A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14105337



Internal ID4088985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41163000..41185237hg38UCSC Ensembl
Innerchr11:41163500..41184737hg38UCSC Ensembl
Outerchr11:41162000..41186237hg38UCSC Ensembl
chr11:41184550..41206787hg19UCSC Ensembl
Innerchr11:41185050..41206287hg19UCSC Ensembl
Outerchr11:41183550..41207787hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3822238
hg1922238
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626084
Supporting Variants
SamplesHG03716
Known GenesLRRC4C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14105337
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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