A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412177



Internal ID22470047
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 StatusS
Merged Variantsnsv5903390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412177
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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