A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023961



Internal ID83686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88428552..88437000hg38UCSC Ensembl
chr9:91043467..91051915hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg388449
hg198449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482708
Supporting Variants
Samples
Known GenesSPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023961
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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