A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028116



Internal ID21937459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68397667..68397724hg38UCSC Ensembl
chr15:68690006..68690063hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607481
Samples
Known GenesITGA11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028116
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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