A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603083



Internal ID6990115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:167873938..167936583hg38UCSC Ensembl
chr4:168795089..168857734hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3862646
hg1962646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11686500, essv11686503, essv11686497, essv11686498, essv11686508, essv11686499, essv11686495, essv11686505, essv11686507, essv11686502, essv11686501, essv11686493, essv11686504, essv11686491, essv11686490, essv11686506, essv11686494, essv11686492, essv11686496
SamplesNA19704, HG02419, HG03130, HG03452, NA19197, HG02420, NA18908, HG02879, HG01187, NA18934, NA19184, NA18856, HG03109, HG02010, HG03103, HG02938, NA19713, NA19213, NA19129
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603083
Frequency
Sample Size2504
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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