A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162708



Internal ID21466238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83092868..83092868hg38UCSC Ensembl
chr9:85707783..85707783hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633503
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162708
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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