A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626082



Internal ID7012916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41096010..41147832hg38UCSC Ensembl
Innerchr11:41096010..41147832hg38UCSC Ensembl
Outerchr11:41095510..41148332hg38UCSC Ensembl
chr11:41117560..41169382hg19UCSC Ensembl
Innerchr11:41117560..41169382hg19UCSC Ensembl
Outerchr11:41117060..41169882hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3851823
hg1951823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv193e214
Supporting Variantsessv14105335, essv14105334
SamplesNA18532, HG03708
Known GenesLRRC4C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626082
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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