A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261902



Internal ID20828942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19976405..19977312hg38UCSC Ensembl
chr3:20017897..20018804hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547881
Supporting Variants
Samples
Known GenesRAB5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261902
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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