A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829220



Internal ID22604155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22173260..22182835hg38UCSC Ensembl
chr1:22499753..22509328hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg389576
hg199576
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829220
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