A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098862



Internal ID21484184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:858458..858458hg38UCSC Ensembl
chr16:908458..908458hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652873
Supporting Variants
SamplesNA12329
Known GenesLMF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098862
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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