A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492814



Internal ID22550742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119575442..119577195hg38UCSC Ensembl
chr4:120496597..120498350hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381754
hg191754
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837636
Supporting Variants
Samples
Known GenesPDE5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492814
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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