A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182214



Internal ID20749254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79964143..80127537hg38UCSC Ensembl
chr15:80256485..80419879hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38163395
hg19163395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497353
Supporting Variants
Samples
Known GenesBCL2A1, ZFAND6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182214
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