A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657583



Internal ID21605888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55258090..55258090hg38UCSC Ensembl
chr16:55292002..55292002hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg381428
hg191428
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091946
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657583
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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