A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5582266



Internal ID21530777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19334912..19334972hg38UCSC Ensembl
chr6:19335143..19335203hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145135
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5582266
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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