A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834129



Internal ID22609064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:94193119..94196587hg38UCSC Ensembl
chr9:42812551..42815212hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg383469
hg192662
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488674, nssv17482372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834129
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