A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625895



Internal ID7012729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33775759..33780448hg38UCSC Ensembl
Innerchr11:33775759..33780448hg38UCSC Ensembl
Outerchr11:33775594..33780605hg38UCSC Ensembl
chr11:33797305..33801994hg19UCSC Ensembl
Innerchr11:33797305..33801994hg19UCSC Ensembl
Outerchr11:33797140..33802151hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384690
hg194690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14088429, essv14088428
SamplesHG00452, HG00657
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625895
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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