A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275545



Internal ID20484763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94686913..94686913hg38UCSC Ensembl
chr9:97449195..97449195hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751250
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275545
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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