A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105094



Internal ID21464474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46735455..46735455hg38UCSC Ensembl
chr19:47238712..47238712hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647785
Supporting Variants
SamplesHG03065
Known GenesSTRN4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105094
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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