A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223336



Internal ID20790376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49745379..49746020hg38UCSC Ensembl
chr13:50319515..50320156hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592893
Supporting Variants
Samples
Known GenesKPNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223336
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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