A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245052



Internal ID20812092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12289665..12290404hg38UCSC Ensembl
chr19:12400480..12401219hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38740
hg19740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598757
Supporting Variants
Samples
Known GenesZNF44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245052
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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