A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11692374



Internal ID2235962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170237457..170344306hg38UCSC Ensembl
chr4:171158608..171265457hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38106850
hg19106850
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603135
Supporting Variants
SamplesHG02009
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11692374
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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