A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247576



Internal ID20814616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17018776..17019269hg38UCSC Ensembl
chr19:17129586..17130079hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599517
Supporting Variants
Samples
Known GenesCPAMD8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247576
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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