A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231597



Internal ID20798638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31975173..31976492hg38UCSC Ensembl
chr13:32549310..32550629hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg381320
hg191320
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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