A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968546



Internal ID22743481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79156823..79156823hg38UCSC Ensembl
chr16:79190720..79190720hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376140
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968546
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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