A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598776



Internal ID6985911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176803319..176875295hg38UCSC Ensembl
chr3:176521107..176593083hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3871977
hg1971977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11236196
SamplesNA19740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598776
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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