A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026592



Internal ID20593632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72582998..72583501hg38UCSC Ensembl
chr15:72875339..72875842hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38504
hg19504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504541
Supporting Variants
Samples
Known GenesARIH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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