A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163206



Internal ID21428996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87818955..87818955hg38UCSC Ensembl
chr9:90433870..90433870hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644457
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163206
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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