A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084060



Internal ID21449941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75115056..75115113hg38UCSC Ensembl
chr14:75581759..75581816hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589293
Supporting Variants
SamplesHG01114
Known GenesNEK9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084060
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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