A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899019



Internal ID22674145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18913442..18979738hg38UCSC Ensembl
chr6:18913673..18979969hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3866297
hg1966297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899019
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