A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv558e214



Internal ID22756452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5868212..5888585hg38UCSC Ensembl
chr17:5771532..5791905hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3820374
hg1920374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3639823, esv3639824
SamplesNA20533, HG03919
Known GenesLOC339166
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv558e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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