A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599696



Internal ID21791742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63127146..63129169hg38UCSC Ensembl
chr15:63419345..63421368hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg382024
hg192024
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6032004
Supporting Variants
Samples
Known GenesLACTB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599696
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