A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970427



Internal ID22745362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20770935..20970953hg38UCSC Ensembl
chr19:20953741..21153759hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38200019
hg19200019
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1020n209
Supporting Variantsnssv17406005
Samples
Known GenesZNF85
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970427
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer