A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162775



Internal ID21483393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70469094..70469094hg38UCSC Ensembl
chr9:73084010..73084010hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639860
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162775
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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