A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833332



Internal ID22608267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58045679..58050809hg38UCSC Ensembl
chr2:58272814..58277944hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg385131
hg195131
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1146n209
Supporting Variantsnssv17487491
Samples
Known GenesVRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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