A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085196



Internal ID21490907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:397709..397709hg38UCSC Ensembl
chr16:447709..447709hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657588
Supporting Variants
SamplesNA19238
Known GenesNME4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085196
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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