A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17105421



Internal ID21407801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46078805..46078805hg38UCSC Ensembl
chr19:46582063..46582063hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657952
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17105421
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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