A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632309



Internal ID21580614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163321366..163321366hg38UCSC Ensembl
chr6:163742398..163742398hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157025
SamplesNA19238
Known GenesPACRG-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632309
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