A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063938



Internal ID21973171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32397296..32397296hg38UCSC Ensembl
chr3:32438788..32438788hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545394
Samples
Known GenesCMTM7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063938
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