A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594605



Internal ID21786648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90467447..90467510hg38UCSC Ensembl
chr9:93229729..93229792hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015658
Supporting Variants
Samples
Known GenesLOC340515
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594605
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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