A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473959



Internal ID22531853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20944982..20946481hg38UCSC Ensembl
chr19:21127788..21129287hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875113
Supporting Variants
Samples
Known GenesZNF85
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473959
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