A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287262



Internal ID20496480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67246645..67246713hg38UCSC Ensembl
chr15:67538983..67539051hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735927
Supporting Variants
Samples
Known GenesAAGAB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287262
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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