A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14105332



Internal ID4077640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40977521..41107744hg38UCSC Ensembl
Innerchr11:40977521..41107744hg38UCSC Ensembl
Outerchr11:40977021..41108244hg38UCSC Ensembl
chr11:40999071..41129294hg19UCSC Ensembl
Innerchr11:40999071..41129294hg19UCSC Ensembl
Outerchr11:40998571..41129794hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38130224
hg19130224
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626080
Supporting Variants
SamplesHG03708
Known GenesLRRC4C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14105332
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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