A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195587



Internal ID20762627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8401555..8401880hg38UCSC Ensembl
chr9:8401555..8401880hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432326
Supporting Variants
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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