A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18246501



Internal ID20813541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8228708..8229574hg38UCSC Ensembl
chr19:8293592..8294458hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597862
Supporting Variants
Samples
Known GenesCERS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18246501
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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