A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162947



Internal ID21428873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90106396..90106478hg38UCSC Ensembl
chr9:92868678..92868760hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600025
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162947
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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