A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260479



Internal ID20827519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170071349..170072230hg38UCSC Ensembl
chr3:169789137..169790018hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38882
hg19882
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570655
Supporting Variants
Samples
Known GenesGPR160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260479
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00027


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