A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268926



Internal ID20835966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59613768..59627849hg38UCSC Ensembl
chr5:58909594..58923675hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3814082
hg1914082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558020
Supporting Variants
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268926
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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