A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625867



Internal ID7012701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32846854..32850966hg38UCSC Ensembl
Innerchr11:32846854..32850966hg38UCSC Ensembl
Outerchr11:32846746..32851078hg38UCSC Ensembl
chr11:32868400..32872512hg19UCSC Ensembl
Innerchr11:32868400..32872512hg19UCSC Ensembl
Outerchr11:32868292..32872624hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384113
hg194113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14084341, essv14084340
SamplesNA19036, NA19316
Known GenesPRRG4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625867
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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