A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602299



Internal ID6989333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133999957..134149092hg38UCSC Ensembl
chr4:134921112..135070247hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38149136
hg19149136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11614047, essv11614048
SamplesNA20768, HG01357
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602299
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer