A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11734112



Internal ID2567345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38n/a
hg19n/a
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variants
Supporting Variants
SamplesHG02278
Known GenesACSL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11734112
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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