A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951856



Internal ID22727197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63988664..63988664hg38UCSC Ensembl
chr8:64901221..64901221hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951856
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer