A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929083



Internal ID21349154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22125189..22125189hg38UCSC Ensembl
chr18:19705150..19705150hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185547
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929083
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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