A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106899



Internal ID21472407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9680230..9680280hg38UCSC Ensembl
chr19:9790906..9790956hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601082
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106899
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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