A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599441



Internal ID6986488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3904368..3991525hg38UCSC Ensembl
chr4:3906095..3993252hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3887158
hg1987158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11317821, essv11317819, essv11317820
SamplesHG02628, HG00346, HG02180
Known GenesFAM86EP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599441
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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