A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832237



Internal ID22607172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230548341..230553488hg38UCSC Ensembl
chr2:231413056..231418203hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg385148
hg195148
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832237
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer