A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832078



Internal ID22607013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183174809..183176311hg38UCSC Ensembl
chr2:184039537..184041039hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg381503
hg191503
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481276, nssv17488758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832078
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