A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584216



Internal ID21776259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108460635..108460635hg38UCSC Ensembl
chr9:111222915..111222915hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38944
hg19944
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584216
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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