A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104608



Internal ID21442265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35527213..35527213hg38UCSC Ensembl
chr19:36018115..36018115hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652418
Supporting Variants
SamplesHG00732
Known GenesSBSN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104608
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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