A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv877e214



Internal ID22756771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21843899..21869016hg38UCSC Ensembl
chr3:21885391..21910508hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3825118
hg1925118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595527, esv3595526
SamplesHG01366, HG03744
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv877e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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