A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596419



Internal ID6983734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65455386..65468786hg38UCSC Ensembl
Innerchr3:65455886..65468286hg38UCSC Ensembl
Outerchr3:65454386..65469786hg38UCSC Ensembl
chr3:65441061..65454461hg19UCSC Ensembl
Innerchr3:65441561..65453961hg19UCSC Ensembl
Outerchr3:65440061..65455461hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3813401
hg1913401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11030290
SamplesNA12342
Known GenesMAGI1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596419
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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