A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028786



Internal ID86897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128251121..128251182hg38UCSC Ensembl
chr9:131013400..131013461hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480464
Supporting Variants
Samples
Known GenesDNM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028786
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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