A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083991



Internal ID21461518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55143843..55143843hg38UCSC Ensembl
chr14:55610561..55610561hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654378
Supporting Variants
SamplesHG02818
Known GenesLGALS3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083991
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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