A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105001



Internal ID21427285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40117180..40119394hg38UCSC Ensembl
chr19:40623087..40625301hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382215
hg192215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598408
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105001
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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