A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv878e214



Internal ID22756772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24703958..24784823hg38UCSC Ensembl
chr3:24745449..24826314hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3880866
hg1980866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595587, esv3595586
SamplesNA19035, NA19321, NA18620
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv878e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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