A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085544



Internal ID21445771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23875580..23875580hg38UCSC Ensembl
chr16:23886901..23886901hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652483
Supporting Variants
SamplesHG00732
Known GenesPRKCB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085544
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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