A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245095



Internal ID20812135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13322046..13322662hg38UCSC Ensembl
chr19:13432860..13433476hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599665
Supporting Variants
Samples
Known GenesCACNA1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245095
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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