A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633606



Internal ID21581911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51735687..51735687hg38UCSC Ensembl
chr10:53495447..53495447hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070645
SamplesNA24385
Known GenesPRKG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633606
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