A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163293



Internal ID21493258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:998541..998638hg38UCSC Ensembl
chr9:998541..998638hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584583
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163293
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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