A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832163



Internal ID22607098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207618555..207626561hg38UCSC Ensembl
chr2:208483279..208491285hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg388007
hg198007
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482036
Samples
Known GenesMETTL21A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832163
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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