A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401205



Internal ID22459075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21972979..22180645hg38UCSC Ensembl
chr19:22155781..22363447hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38207667
hg19207667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938160
Supporting Variants
Samples
Known GenesZNF208, ZNF257, ZNF676
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401205
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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