A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595962



Internal ID6983280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41028388..41031855hg38UCSC Ensembl
Innerchr3:41028388..41031855hg38UCSC Ensembl
Outerchr3:41028193..41032046hg38UCSC Ensembl
chr3:41069879..41073346hg19UCSC Ensembl
Innerchr3:41069879..41073346hg19UCSC Ensembl
Outerchr3:41069684..41073537hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg383468
hg193468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10989676
SamplesHG01986
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595962
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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