A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598906



Internal ID6985954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182340260..182350246hg38UCSC Ensembl
Innerchr3:182340260..182350246hg38UCSC Ensembl
Outerchr3:182340052..182350341hg38UCSC Ensembl
chr3:182058048..182068034hg19UCSC Ensembl
Innerchr3:182058048..182068034hg19UCSC Ensembl
Outerchr3:182057840..182068129hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg389987
hg199987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11251458
SamplesNA18965
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598906
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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