A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550390



Internal ID21874745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196938648..196938648hg38UCSC Ensembl
chr3:196665519..196665519hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068040
Supporting Variants
Samples
Known GenesNCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550390
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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