A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104785



Internal ID21506535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36126419..36126419hg38UCSC Ensembl
chr19:36617321..36617321hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382121
hg192121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644711
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104785
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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