A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602922



Internal ID6989955
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11672453
SamplesHG01398
Known GenesFSTL5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602922
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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