A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651299



Internal ID21599604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29103620..29103620hg38UCSC Ensembl
chr14:29572826..29572826hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091961
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651299
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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