A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640608



Internal ID21588913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8617402..8617402hg38UCSC Ensembl
chr8:8474912..8474912hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148149
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640608
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