A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599416



Internal ID6639680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2972522..3012111hg38UCSC Ensembl
chr4:2974249..3013838hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3839590
hg1939590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11317191, essv11317190
SamplesHG01610, HG00732
Known GenesGRK4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599416
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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