A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259998



Internal ID20827038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37265950..37266176hg38UCSC Ensembl
chr3:37307441..37307667hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536392
Supporting Variants
Samples
Known GenesGOLGA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259998
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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