A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635076



Internal ID21583381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14657156..14657156hg38UCSC Ensembl
chr6:14657387..14657387hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150465
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635076
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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