A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068372



Internal ID21414623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11478911..11478911hg38UCSC Ensembl
chr10:11520910..11520910hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626643
Supporting Variants
SamplesHG00513
Known GenesUSP6NL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068372
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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