A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602284



Internal ID6989318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133441311..133450148hg38UCSC Ensembl
Innerchr4:133441361..133450098hg38UCSC Ensembl
Outerchr4:133441261..133450198hg38UCSC Ensembl
chr4:134362466..134371303hg19UCSC Ensembl
Innerchr4:134362516..134371253hg19UCSC Ensembl
Outerchr4:134362416..134371353hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg388838
hg198838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11612197
SamplesHG01362
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602284
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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