A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562968



Internal ID20936039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160046654..160345667hg38UCSC Ensembl
chr3:159764441..160063455hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38299014
hg19299015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259828
Samples
Known GenesC3orf80, IFT80, IL12A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562968
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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