A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596447



Internal ID6983762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67034534..67091368hg38UCSC Ensembl
chr3:67084958..67141792hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3856835
hg1956835
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv899e214
Supporting Variantsessv11030919, essv11030918
SamplesHG00524, NA20822
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596447
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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