A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv990e214



Internal ID22756884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16421889..16427961hg38UCSC Ensembl
chr4:16423512..16429584hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg386073
hg196073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3599758, esv3599757
SamplesHG01443, HG00330, NA11831
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv990e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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