A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261901



Internal ID20828941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19974204..19975163hg38UCSC Ensembl
chr3:20015696..20016655hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38960
hg19960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552470
Supporting Variants
Samples
Known GenesRAB5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261901
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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