A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1127e214



Internal ID22757021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113620657..113657234hg38UCSC Ensembl
chr5:112956354..112992931hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3836578
hg1936578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3606322, esv3606321
SamplesHG03777, HG03973
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1127e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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