A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11690415



Internal ID988865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169759884..169762716hg38UCSC Ensembl
Innerchr4:169759938..169762662hg38UCSC Ensembl
Outerchr4:169759830..169762770hg38UCSC Ensembl
chr4:170681035..170683867hg19UCSC Ensembl
Innerchr4:170681089..170683813hg19UCSC Ensembl
Outerchr4:170680981..170683921hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg382833
hg192833
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603126
Supporting Variants
SamplesHG00614
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11690415
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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