A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626524



Internal ID7013356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58832286..58836413hg38UCSC Ensembl
chr11:58599759..58603886hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg384128
hg194128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14173740, essv14173741, essv14173743, essv14173739, essv14173742
SamplesHG02573, HG02678, HG02878, HG02759, HG02861
Known GenesGLYATL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626524
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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