A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625539



Internal ID7012373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19655426..19663918hg38UCSC Ensembl
Innerchr11:19655426..19663918hg38UCSC Ensembl
Outerchr11:19655156..19664202hg38UCSC Ensembl
chr11:19676972..19685464hg19UCSC Ensembl
Innerchr11:19676972..19685464hg19UCSC Ensembl
Outerchr11:19676702..19685748hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg388493
hg198493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14046194
SamplesHG00581
Known GenesNAV2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625539
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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