A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246477



Internal ID20813517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7746779..7749975hg38UCSC Ensembl
chr19:7811665..7814861hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383197
hg193197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599476
Supporting Variants
Samples
Known GenesCD209
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246477
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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