A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027045



Internal ID85751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104124293..104124375hg38UCSC Ensembl
chr9:106886574..106886656hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489859
Supporting Variants
Samples
Known GenesSMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027045
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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