A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610488



Internal ID6997405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117186918..117241471hg38UCSC Ensembl
chr6:117508081..117562634hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3854554
hg1954554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12513053, essv12513052, essv12513054
SamplesNA18861, HG03091, HG03538
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610488
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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