A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626548



Internal ID6666698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60085948..60101194hg38UCSC Ensembl
chr11:59853421..59868667hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3815247
hg1915247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv201e214
Supporting Variantsessv14174901, essv14174899, essv14174902, essv14174900
SamplesNA18864, HG03786, NA18946, NA18952
Known GenesMS4A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626548
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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