A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161593



Internal ID21465798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32273603..32273711hg38UCSC Ensembl
chr9:32273601..32273709hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603865
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161593
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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