A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3594900



Internal ID6635175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:328751..540780hg38UCSC Ensembl
chr3:370434..582463hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38212030
hg19212030
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10897488
SamplesHG02238
Known GenesCHL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3594900
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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