A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094463



Internal ID21473389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77117089..77117089hg38UCSC Ensembl
chr14:77583432..77583432hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645136
Supporting Variants
SamplesHG03371
Known GenesKIAA1737
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094463
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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