A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1146n209



Internal ID22827221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58045529..58050809hg38UCSC Ensembl
chr2:58272664..58277944hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg385281
hg195281
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5833071, nsv5833332
Samples
Known GenesVRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1146n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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