A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv899e214



Internal ID22756793
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 Variants
Supporting Variantsesv3596447, esv3596448
SamplesHG00524, NA20822
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv899e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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