A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625213



Internal ID7012048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5195168..5224501hg38UCSC Ensembl
chr11:5216398..5245731hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3829334
hg1929334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv182e214
Supporting Variantsessv14003261, essv14003262
SamplesHG03476, HG00581
Known GenesOR51V1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625213
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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