A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832361



Internal ID22607296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:199482120..199486056hg38UCSC Ensembl
chr2:200346843..200350779hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg383937
hg193937
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832361
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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