A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483658



Internal ID261094
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 StatusM
Merged Variants
Supporting Variantsnssv17028551
Samples
Known GenesGGTA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483658
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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