A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968285



Internal ID22743221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59410554..59410554hg38UCSC Ensembl
chr18:57077786..57077786hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968285
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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