A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260259



Internal ID20827299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132708998..132710676hg38UCSC Ensembl
chr3:132427842..132429520hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381679
hg191679
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566356
Supporting Variants
Samples
Known GenesNPHP3, NPHP3-ACAD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260259
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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