A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625768



Internal ID6665916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27328141..27335102hg38UCSC Ensembl
Innerchr11:27328141..27335102hg38UCSC Ensembl
Outerchr11:27327641..27335602hg38UCSC Ensembl
chr11:27349688..27356649hg19UCSC Ensembl
Innerchr11:27349688..27356649hg19UCSC Ensembl
Outerchr11:27349188..27357149hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg386962
hg196962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14071738, essv14071737
SamplesNA20858, HG03653
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625768
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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