A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105677



Internal ID22014910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34436515..34436515hg38UCSC Ensembl
chr18:32016479..32016479hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622082
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105677
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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