A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599118



Internal ID6986166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191634598..191712717hg38UCSC Ensembl
chr3:191352387..191430506hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3878120
hg1978120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv965e214
Supporting Variantsessv11272667, essv11272666
SamplesHG03713, HG00371
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599118
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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