A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520705



Internal ID297023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2820891..2825477hg38UCSC Ensembl
chr19:2820889..2825475hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384587
hg194587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv237n206
Supporting Variantsnssv17720462
Samples
Known GenesZNF554
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520705
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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