A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655809



Internal ID21604114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36119591..36119591hg38UCSC Ensembl
chr18:33699554..33699554hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100886
SamplesHG03065
Known GenesSLC39A6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655809
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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