A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600696



Internal ID6987736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62088230..62092792hg38UCSC Ensembl
Innerchr4:62088263..62092760hg38UCSC Ensembl
Outerchr4:62088198..62092825hg38UCSC Ensembl
chr4:62953948..62958510hg19UCSC Ensembl
Innerchr4:62953981..62958478hg19UCSC Ensembl
Outerchr4:62953916..62958543hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg384563
hg194563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11455287
SamplesHG03133
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600696
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