A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595937



Internal ID6983255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39769528..39780124hg38UCSC Ensembl
Innerchr3:39769528..39780124hg38UCSC Ensembl
Outerchr3:39769028..39780624hg38UCSC Ensembl
chr3:39811019..39821615hg19UCSC Ensembl
Innerchr3:39811019..39821615hg19UCSC Ensembl
Outerchr3:39810519..39822115hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3810597
hg1910597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10987885
SamplesNA20812
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595937
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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