A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903390



Internal ID22678557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16858235..16858286hg38UCSC Ensembl
chr6:16858466..16858517hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903390
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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