A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586974



Internal ID21779017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16805460..16805584hg38UCSC Ensembl
chr9:16805458..16805582hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015861
Supporting Variants
Samples
Known GenesBNC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586974
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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