A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955800



Internal ID22730998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87746557..87746557hg38UCSC Ensembl
chr9:90361472..90361472hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955800
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer