A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581543



Internal ID21530043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18002026..18002077hg38UCSC Ensembl
chr8:17859535..17859586hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150738
SamplesHG03065
Known GenesPCM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581543
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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