A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107215



Internal ID20674255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119627101..119627600hg38UCSC Ensembl
chr4:120548256..120548755hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391403
Supporting Variants
Samples
Known GenesPDE5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107215
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08479


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