A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897119



Internal ID22672217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122331696..122372143hg38UCSC Ensembl
chr6:122652841..122693288hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3840448
hg1940448
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897119
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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