A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832076



Internal ID22607011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:182645083..182671113hg38UCSC Ensembl
chr2:183509810..183535840hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3826031
hg1926031
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481271
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832076
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