A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163393



Internal ID21412186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91385878..91386199hg38UCSC Ensembl
chr9:94148160..94148481hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603112
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163393
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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