A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17106571



Internal ID21476233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8247735..8247735hg38UCSC Ensembl
chr19:8312619..8312619hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382790
hg192790
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653545
Supporting Variants
SamplesHG03486
Known GenesCERS4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17106571
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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