A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103804



Internal ID22013037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:667491..667491hg38UCSC Ensembl
chr18:667491..667491hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622932
Samples
Known GenesTYMS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103804
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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