A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581991



Internal ID21774034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108231011..108232029hg38UCSC Ensembl
chr9:110993291..110994309hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017231
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581991
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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