A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644565



Internal ID21592870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99285320..99285320hg38UCSC Ensembl
chr14:99751657..99751657hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094645
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644565
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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