A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644925



Internal ID21593230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35375522..35375522hg38UCSC Ensembl
chr14:35844728..35844728hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381745
hg191745
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096178
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644925
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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