A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1131e214



Internal ID22757025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117619204..117647595hg38UCSC Ensembl
chr5:116954899..116983290hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3828392
hg1928392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3606432, esv3606431
SamplesNA21142
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1131e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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