A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088763



Internal ID21459525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104685973..104685973hg38UCSC Ensembl
chr14:105152310..105152310hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645479
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088763
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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