A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178180



Internal ID20745220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78126291..78145420hg38UCSC Ensembl
chr15:78418633..78437762hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3819130
hg1919130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513216
Supporting Variants
Samples
Known GenesCIB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178180
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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