A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261712



Internal ID20470930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88974406..88974406hg38UCSC Ensembl
chr9:91589321..91589321hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261712
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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