A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105015



Internal ID22014249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59271499..59271499hg38UCSC Ensembl
chr18:56938731..56938731hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627817
Samples
Known GenesRAX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105015
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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