A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907722



Internal ID22682932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168789855..168966841hg38UCSC Ensembl
chr6:169189950..169366936hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38176987
hg19176987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907722
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