A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11170534



Internal ID1548146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145504279..145551010hg38UCSC Ensembl
chr3:145222066..145268797hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3846732
hg1946732
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598066
Supporting Variants
SamplesHG01432
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11170534
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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