A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599113



Internal ID21791158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64539519..64543473hg38UCSC Ensembl
chr15:64831718..64835672hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383955
hg193955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6023990
Supporting Variants
Samples
Known GenesZNF609
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599113
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