A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589086



Internal ID21537650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87858623..87860001hg38UCSC Ensembl
chr10:89618380..89619758hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg381379
hg191379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071748
SamplesNA19238
Known GenesKLLN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589086
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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