A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649909



Internal ID21598214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62126380..62126380hg38UCSC Ensembl
chr16:62160284..62160284hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089914
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649909
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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