A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1152e214



Internal ID22757046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162183062..162215988hg38UCSC Ensembl
chr5:161610068..161642994hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3832927
hg1932927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3607422, esv3607420
SamplesHG03709, HG01705
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1152e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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