A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652222



Internal ID21600527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20609084..20609084hg38UCSC Ensembl
chr14:21077243..21077243hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081291
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652222
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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