A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571472



Internal ID21519851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124837751..124837803hg38UCSC Ensembl
chr8:125849993..125850045hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141840
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571472
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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