A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635209



Internal ID21583514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160282966..160282966hg38UCSC Ensembl
chr5:159709973..159709973hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131588
SamplesNA19239
Known GenesCCNJL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635209
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