A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162496



Internal ID21511051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80792668..80792668hg38UCSC Ensembl
chr9:83407583..83407583hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633193
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162496
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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