A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261185



Internal ID20828225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180906814..180907148hg38UCSC Ensembl
chr3:180624602..180624936hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261185
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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