A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162609



Internal ID21466207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68284621..68284621hg38UCSC Ensembl
chr9:70899537..70899537hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642511
Supporting Variants
SamplesHG03065
Known GenesCBWD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162609
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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