A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv874e214



Internal ID22756768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20972954..20977119hg38UCSC Ensembl
chr3:21014446..21018611hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384166
hg194166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595495, esv3595496
SamplesNA20531, NA20764, HG01613, HG03694
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv874e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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