A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092936



Internal ID21470126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79156823..79156823hg38UCSC Ensembl
chr16:79190720..79190720hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644633
Supporting Variants
SamplesHG03125
Known GenesWWOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092936
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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