A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581908



Internal ID21530413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21851442..21851620hg38UCSC Ensembl
chr6:21851673..21851851hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150488
SamplesNA12878
Known GenesCASC15
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581908
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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