A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579213



Internal ID21771256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97411017..97411125hg38UCSC Ensembl
chr9:100173299..100173407hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001941
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579213
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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