A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584830



Internal ID21533374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132377307..132377429hg38UCSC Ensembl
chr9:135252694..135252816hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160385
SamplesHG00512
Known GenesTTF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584830
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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