A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185182



Internal ID20752222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64426603..64427103hg38UCSC Ensembl
chr15:64718802..64719302hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497677
Supporting Variants
Samples
Known GenesTRIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185182
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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