A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13765143



Internal ID3766959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44993759..45028111hg38UCSC Ensembl
chr10:45489207..45523559hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3834353
hg1934353
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623079
Supporting Variants
SamplesHG03380
Known GenesC10orf25, RASSF4, ZNF22
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13765143
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