A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105258



Internal ID21459230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43873778..43873778hg38UCSC Ensembl
chr19:44377930..44377930hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg381890
hg191890
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660461
Supporting Variants
SamplesHG02818
Known GenesZNF404
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105258
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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