A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599096



Internal ID21547729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113700868..113701072hg38UCSC Ensembl
chr9:116463148..116463352hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159848
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599096
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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