A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11023640



Internal ID4462383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59740123..59744599hg38UCSC Ensembl
Innerchr3:59740139..59744583hg38UCSC Ensembl
Outerchr3:59740107..59744615hg38UCSC Ensembl
chr3:59725849..59730325hg19UCSC Ensembl
Innerchr3:59725865..59730309hg19UCSC Ensembl
Outerchr3:59725833..59730341hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg384477
hg194477
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596285
Supporting Variants
SamplesHG03968
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11023640
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