A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11672453



Internal ID1525497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:161961623..162024651hg38UCSC Ensembl
Innerchr4:161961623..162024651hg38UCSC Ensembl
Outerchr4:161961123..162025151hg38UCSC Ensembl
chr4:162882775..162945803hg19UCSC Ensembl
Innerchr4:162882775..162945803hg19UCSC Ensembl
Outerchr4:162882275..162946303hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3863029
hg1963029
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602922
Supporting Variants
SamplesHG01398
Known GenesFSTL5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11672453
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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