A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550948



Internal ID21875303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195771275..195771275hg38UCSC Ensembl
chr3:195498146..195498146hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079975
Supporting Variants
Samples
Known GenesMUC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550948
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