A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603523



Internal ID6990554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186176579..186214960hg38UCSC Ensembl
chr4:187097733..187136114hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3838382
hg1938382
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11744404, essv11744406, essv11744405, essv11744410, essv11744412, essv11744409, essv11744411, essv11744407, essv11744408
SamplesHG03731, HG02727, HG04156, HG04183, HG03771, HG04180, HG03951, NA20847, HG03864
Known GenesCYP4V2, FLJ38576
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603523
Frequency
Sample Size2504
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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