A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163118



Internal ID21403431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89212781..89217529hg38UCSC Ensembl
chr9:91827696..91832444hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg384749
hg194749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591429
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163118
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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