A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837636



Internal ID22612571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119575442..119577195hg38UCSC Ensembl
chr4:120496597..120498350hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381754
hg191754
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1591n209
Supporting Variantsnssv17492814
Samples
Known GenesPDE5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837636
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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