A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659224



Internal ID21607529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77220916..77220916hg38UCSC Ensembl
chr14:77687259..77687259hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090377, nssv17082496
SamplesNA24385, HG00513
Known GenesTMEM63C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659224
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer