A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595545



Internal ID6982863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22395753..22409441hg38UCSC Ensembl
Innerchr3:22396253..22408941hg38UCSC Ensembl
Outerchr3:22394753..22410441hg38UCSC Ensembl
chr3:22437244..22450932hg19UCSC Ensembl
Innerchr3:22437744..22450432hg19UCSC Ensembl
Outerchr3:22436244..22451932hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3813689
hg1913689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10948600
SamplesNA19782
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595545
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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