A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959600



Internal ID22734622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77916904..77916904hg38UCSC Ensembl
chr10:79676662..79676662hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360866
Samples
Known GenesDLG5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959600
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