A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089092



Internal ID21506548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49953093..49953093hg38UCSC Ensembl
chr16:49987004..49987004hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662744
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089092
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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