A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722161



Internal ID145827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20045607..20884415hg38UCSC Ensembl
chr19:20156416..21067221hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38838809
hg19910806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532523
Supporting Variants
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF626, ZNF737, ZNF826P, ZNF90
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722161
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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