A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596262



Internal ID6983579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59037102..59066810hg38UCSC Ensembl
Innerchr3:59037129..59066783hg38UCSC Ensembl
Outerchr3:59037075..59066837hg38UCSC Ensembl
chr3:59022828..59052536hg19UCSC Ensembl
Innerchr3:59022855..59052509hg19UCSC Ensembl
Outerchr3:59022801..59052563hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3829709
hg1929709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11023314
SamplesHG02494
Known GenesC3orf67
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596262
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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