A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223742



Internal ID20790782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44996102..44996615hg38UCSC Ensembl
chr13:45570237..45570750hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588419
Supporting Variants
Samples
Known GenesGPALPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223742
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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