A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3594938



Internal ID6635213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:965168..1046488hg38UCSC Ensembl
chr3:1006852..1088172hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3881321
hg1981321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10898248
SamplesHG00264
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3594938
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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