A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829393



Internal ID22604328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231279273..231302798hg38UCSC Ensembl
chr1:231415019..231438544hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3823526
hg1923526
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829393
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