A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432871



Internal ID22490741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33796398..33796481hg38UCSC Ensembl
chr6:33764175..33764258hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899321
Supporting Variants
Samples
Known GenesMLN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432871
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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