A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027803



Internal ID21937146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65267512..65267583hg38UCSC Ensembl
chr15:65559850..65559921hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602456
Samples
Known GenesPARP16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027803
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