A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961878



Internal ID22736819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134785620..134785620hg38UCSC Ensembl
chr3:134504462..134504462hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393067
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961878
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