A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088321



Internal ID21507774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76828676..76828676hg38UCSC Ensembl
chr14:77295019..77295019hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653259
Supporting Variants
SamplesNA20509
Known GenesC14orf166B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088321
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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