A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14105114



Internal ID3507186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40771862..40835183hg38UCSC Ensembl
Innerchr11:40771888..40835157hg38UCSC Ensembl
Outerchr11:40771836..40835209hg38UCSC Ensembl
chr11:40793412..40856733hg19UCSC Ensembl
Innerchr11:40793438..40856707hg19UCSC Ensembl
Outerchr11:40793386..40856759hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3863322
hg1963322
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626074
Supporting Variants
SamplesHG03111
Known GenesLRRC4C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14105114
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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