A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831426



Internal ID22606361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168024845..168050569hg38UCSC Ensembl
chr2:168881355..168907079hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3825725
hg1925725
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488325
Samples
Known GenesSTK39
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831426
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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