A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161903



Internal ID21460161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66018676..66018676hg38UCSC Ensembl
chr9:42502664..42502664hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643628
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161903
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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