A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095343



Internal ID22004576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63287352..63287352hg38UCSC Ensembl
chr15:63579551..63579551hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605505
Samples
Known GenesAPH1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095343
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