A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087531



Internal ID21483444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105739012..105739012hg38UCSC Ensembl
chr14:106205349..106205349hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651297
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087531
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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