A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261755



Internal ID20828795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119837443..119838026hg38UCSC Ensembl
chr3:119556290..119556873hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556967
Supporting Variants
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261755
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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