A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261105



Internal ID20828145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164654444..164656121hg38UCSC Ensembl
chr3:164372232..164373909hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg381678
hg191678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566001
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261105
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00018


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