A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636297



Internal ID21584602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29771253..29771253hg38UCSC Ensembl
chr8:29628769..29628769hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143849
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636297
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