A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960697



Internal ID22735667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137408546..137408546hg38UCSC Ensembl
chr9:140302998..140302998hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430793
Samples
Known GenesEXD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960697
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