A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832266



Internal ID22607201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:240982605..240991800hg38UCSC Ensembl
chr2:241922022..241931217hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg389196
hg199196
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483450
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832266
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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