A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831848



Internal ID22606783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20176565..20179146hg38UCSC Ensembl
chr2:20376326..20378907hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg382582
hg192582
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831848
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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