A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260515



Internal ID20827555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170426972..170427413hg38UCSC Ensembl
chr3:170144760..170145201hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556585
Supporting Variants
Samples
Known GenesCLDN11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260515
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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