A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944165



Internal ID22719625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21973520..22180934hg38UCSC Ensembl
chr19:22156322..22363736hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38207415
hg19207415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1023n209
Supporting Variantsnssv17403876
Samples
Known GenesZNF208, ZNF257, ZNF676
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944165
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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