A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268687



Internal ID20835727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149906450..149906864hg38UCSC Ensembl
chr5:149286013..149286427hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568452
Supporting Variants
Samples
Known GenesPDE6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268687
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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