A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580959



Internal ID21773002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114718137..114718220hg38UCSC Ensembl
chr9:117480417..117480500hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580959
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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