A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11370593



Internal ID4537938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24355085..24359419hg38UCSC Ensembl
Innerchr4:24355101..24359404hg38UCSC Ensembl
Outerchr4:24355070..24359435hg38UCSC Ensembl
chr4:24356708..24361042hg19UCSC Ensembl
Innerchr4:24356724..24361027hg19UCSC Ensembl
Outerchr4:24356693..24361058hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg384335
hg194335
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599940
Supporting Variants
SamplesHG04033
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11370593
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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