A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515656



Internal ID292135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9381965..9382040hg38UCSC Ensembl
chr19:9492641..9492716hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721222
Samples
Known GenesZNF177, ZNF559-ZNF177
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515656
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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