A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163450



Internal ID21493235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98636179..98636179hg38UCSC Ensembl
chr9:101398461..101398461hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630677
Supporting Variants
SamplesNA19238
Known GenesGABBR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163450
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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