A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596386



Internal ID6636657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63002548..63210981hg38UCSC Ensembl
chr3:62988224..63196657hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38208434
hg19208434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11026596, essv11026597
SamplesHG03096, HG03577
Known GenesLINC00698
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596386
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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