A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261349



Internal ID20828389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31026595..31026785hg38UCSC Ensembl
chr3:31068087..31068277hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261349
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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