A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625124



Internal ID7011962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2276462..2289805hg38UCSC Ensembl
Innerchr11:2276464..2289804hg38UCSC Ensembl
Outerchr11:2276461..2289807hg38UCSC Ensembl
chr11:2297692..2311035hg19UCSC Ensembl
Innerchr11:2297694..2311034hg19UCSC Ensembl
Outerchr11:2297691..2311037hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3813344
hg1913344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13993599, essv13993600
SamplesHG00879, HG02048
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625124
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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