A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833071



Internal ID22608006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58045529..58049528hg38UCSC Ensembl
chr2:58272664..58276663hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1146n209
Supporting Variantsnssv17487489
Samples
Known GenesVRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833071
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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