A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092003



Internal ID21491935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99332360..99332360hg38UCSC Ensembl
chr14:99798697..99798697hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646319
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092003
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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