A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11394487



Internal ID4448034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35962741..35964982hg38UCSC Ensembl
Innerchr4:35962752..35964972hg38UCSC Ensembl
Outerchr4:35962731..35964993hg38UCSC Ensembl
chr4:35964363..35966604hg19UCSC Ensembl
Innerchr4:35964374..35966594hg19UCSC Ensembl
Outerchr4:35964353..35966615hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382242
hg192242
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600214
Supporting Variants
SamplesHG03953
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11394487
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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