A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625713



Internal ID7012547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25535794..25537051hg38UCSC Ensembl
Innerchr11:25535794..25537051hg38UCSC Ensembl
Outerchr11:25535572..25537280hg38UCSC Ensembl
chr11:25557340..25558597hg19UCSC Ensembl
Innerchr11:25557340..25558597hg19UCSC Ensembl
Outerchr11:25557118..25558826hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg381258
hg191258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14063673, essv14063675, essv14063677, essv14063672, essv14063674, essv14063676
SamplesHG00650, HG00451, NA18648, NA18605, NA18546, HG00478
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625713
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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