A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023960



Internal ID83685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88405254..88414545hg38UCSC Ensembl
chr9:91020169..91029460hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg389292
hg199292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491927
Supporting Variants
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023960
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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