A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661292



Internal ID21609597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37997372..37997372hg38UCSC Ensembl
chr14:38466577..38466577hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg382497
hg192497
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098833
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661292
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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