A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598118



Internal ID6985254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147766890..147888706hg38UCSC Ensembl
chr3:147484677..147606493hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38121817
hg19121817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11176503, essv11176505, essv11176504
SamplesHG00151, NA19731, HG00329
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598118
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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