A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592659



Internal ID21541242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33600213..33601844hg38UCSC Ensembl
chr9:33600211..33601842hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381632
hg191632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161962
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592659
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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