A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028551



Internal ID86730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121461075..121468971hg38UCSC Ensembl
chr9:124223353..124231249hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg387897
hg197897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483658
Supporting Variants
Samples
Known GenesGGTA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028551
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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