A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163099



Internal ID21428947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88659607..88659607hg38UCSC Ensembl
chr9:91274522..91274522hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg386009
hg196009
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634129
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163099
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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