A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657044



Internal ID21605349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65297063..65297063hg38UCSC Ensembl
chr16:65330966..65330966hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096240
SamplesNA19983
Known GenesLINC00922
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657044
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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