A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837864



Internal ID22612799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119575316..119576791hg38UCSC Ensembl
chr4:120496471..120497946hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381476
hg191476
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1591n209
Supporting Variantsnssv17492813
Samples
Known GenesPDE5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837864
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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