A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023353



Internal ID21932696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32067248..32098850hg38UCSC Ensembl
chr18:29647211..29678813hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3831603
hg1931603
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617764
Samples
Known GenesRNF125, RNF138
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023353
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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