A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025709



Internal ID20592749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65199342..65220252hg38UCSC Ensembl
chr15:65491680..65512590hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3820911
hg1920911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506452
Supporting Variants
Samples
Known GenesCILP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025709
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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