A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576529



Internal ID21524969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122102869..122102932hg38UCSC Ensembl
chr3:121821716..121821779hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120616
SamplesHG03486
Known GenesCD86
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576529
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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