A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105294



Internal ID22014527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74198906..74198906hg38UCSC Ensembl
chr18:71866141..71866141hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105294
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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