A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261274



Internal ID20828314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187030633..187031780hg38UCSC Ensembl
chr3:186748421..186749568hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381148
hg191148
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562518
Supporting Variants
Samples
Known GenesST6GAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261274
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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