A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589663



Internal ID21538228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87815535..87815602hg38UCSC Ensembl
chr9:90430450..90430517hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163205
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589663
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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