A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024049



Internal ID20591089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52010431..52015309hg38UCSC Ensembl
chr15:52302628..52307506hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg384879
hg194879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507597
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024049
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00038


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