A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11744406



Internal ID1746222
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603523
Supporting Variants
SamplesHG03771
Known GenesCYP4V2, FLJ38576
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11744406
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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