A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725212



Internal ID148878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44005482..44005533hg38UCSC Ensembl
chr19:44509634..44509685hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417520
Supporting Variants
Samples
Known GenesZNF230
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725212
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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