A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1128e214



Internal ID22757022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114139043..114178772hg38UCSC Ensembl
chr5:113474740..113514469hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3839730
hg1939730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3606333, esv3606334
SamplesHG01351, HG01668, NA19720, HG02260, HG01251
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1128e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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