A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160876



Internal ID21406665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13605521..13605521hg38UCSC Ensembl
chr9:13605520..13605520hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632661
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160876
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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