A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11528418



Internal ID4706199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88422587..88426996hg38UCSC Ensembl
Innerchr4:88422591..88426992hg38UCSC Ensembl
Outerchr4:88422583..88427000hg38UCSC Ensembl
chr4:89343739..89348148hg19UCSC Ensembl
Innerchr4:89343743..89348144hg19UCSC Ensembl
Outerchr4:89343735..89348152hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg384410
hg194410
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601304
Supporting Variants
SamplesHG04225
Known GenesHERC6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11528418
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