A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104510



Internal ID21481554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36222838..36222838hg38UCSC Ensembl
chr19:36713740..36713740hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382504
hg192504
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651250
Supporting Variants
SamplesHG03683
Known GenesZNF146
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104510
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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