A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587948



Internal ID21536509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65321900..65321965hg38UCSC Ensembl
chr16:65355803..65355868hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087843
SamplesHG00732
Known GenesLINC00922
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587948
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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