A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833659



Internal ID22608594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58109324..58111873hg38UCSC Ensembl
chr2:58336459..58339008hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg382550
hg192550
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487495
Samples
Known GenesVRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833659
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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