A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598253



Internal ID6985389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154524714..154676983hg38UCSC Ensembl
chr3:154242503..154394772hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38152270
hg19152270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11190135, essv11190132, essv11190131, essv11190134, essv11190133
SamplesHG03280, NA19201, HG03520, HG01956, NA21088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598253
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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