A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651194



Internal ID21599499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60224841..60224841hg38UCSC Ensembl
chr14:60691559..60691559hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084423
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651194
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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