A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406943



Internal ID22464813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11675731..11685503hg38UCSC Ensembl
chr19:11786546..11796318hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg389773
hg199773
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975905
Supporting Variants
Samples
Known GenesZNF833P
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406943
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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