A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259781



Internal ID20826821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141747649..141748538hg38UCSC Ensembl
chr3:141466491..141467380hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555939
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259781
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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