A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261921



Internal ID20828961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20179630..20180037hg38UCSC Ensembl
chr3:20221122..20221529hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541772
Supporting Variants
Samples
Known GenesSGOL1, SGOL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261921
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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