A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977341



Internal ID22752276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20769287..20965951hg38UCSC Ensembl
chr19:20952093..21148757hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38196665
hg19196665
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1020n209
Supporting Variantsnssv17399466
Samples
Known GenesZNF85
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977341
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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