A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178666



Internal ID20745706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96981901..96986800hg38UCSC Ensembl
chr15:97525131..97530030hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512598
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178666
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