A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107205



Internal ID20674245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119504941..119505438hg38UCSC Ensembl
chr4:120426096..120426593hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379528
Supporting Variants
Samples
Known GenesPDE5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107205
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00034


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