A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089160



Internal ID21406427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:858518..858518hg38UCSC Ensembl
chr16:908518..908518hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663851
Supporting Variants
SamplesHG00512
Known GenesLMF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089160
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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