A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562272



Internal ID21886627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47224589..47224589hg38UCSC Ensembl
chr6:47192325..47192325hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg382409
hg192409
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065562
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562272
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