A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082893



Internal ID21483287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100166005..100166005hg38UCSC Ensembl
chr14:100632342..100632342hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655210
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082893
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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