A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261706



Internal ID20828746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116535662..116536662hg38UCSC Ensembl
chr3:116254509..116255509hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556707
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261706
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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