A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596339



Internal ID6983656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61326255..61384575hg38UCSC Ensembl
Innerchr3:61326260..61384570hg38UCSC Ensembl
Outerchr3:61326250..61384580hg38UCSC Ensembl
chr3:61311929..61370249hg19UCSC Ensembl
Innerchr3:61311934..61370244hg19UCSC Ensembl
Outerchr3:61311924..61370254hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3858321
hg1958321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11026101
SamplesHG03887
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596339
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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