A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977389



Internal ID22752324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20812138..20994800hg38UCSC Ensembl
chr19:20994944..21177606hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38182663
hg19182663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1020n209
Supporting Variantsnssv17396963
Samples
Known GenesZNF85
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977389
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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