A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436237



Internal ID22494107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33337248..33349967hg38UCSC Ensembl
chr6:33305025..33317744hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3812720
hg1912720
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891800
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436237
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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