A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260464



Internal ID20827504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169821268..170002422hg38UCSC Ensembl
chr3:169539056..169720210hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38181155
hg19181155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555884
Supporting Variants
Samples
Known GenesLOC100128164, LRRC31, LRRIQ4, SAMD7, SEC62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260464
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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