A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553858



Internal ID21878213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119540992..119542130hg38UCSC Ensembl
chr4:120462147..120463285hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381139
hg191139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5994882
Supporting Variants
Samples
Known GenesPDE5A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553858
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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