A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625118



Internal ID6665269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1872985..1875776hg38UCSC Ensembl
Innerchr11:1872987..1875774hg38UCSC Ensembl
Outerchr11:1872983..1875778hg38UCSC Ensembl
chr11:1894215..1897006hg19UCSC Ensembl
Innerchr11:1894217..1897004hg19UCSC Ensembl
Outerchr11:1894213..1897008hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382792
hg192792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13993514, essv13993513
SamplesHG01029, HG00513
Known GenesLSP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625118
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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