A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625504



Internal ID7012338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18579081..18583137hg38UCSC Ensembl
Innerchr11:18579131..18583087hg38UCSC Ensembl
Outerchr11:18579031..18583187hg38UCSC Ensembl
chr11:18600628..18604684hg19UCSC Ensembl
Innerchr11:18600678..18604634hg19UCSC Ensembl
Outerchr11:18600578..18604734hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384057
hg194057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14043309
SamplesHG02031
Known GenesUEVLD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625504
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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