A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038041



Internal ID21947384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23615665..23623933hg38UCSC Ensembl
chr18:21195629..21203897hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg388269
hg198269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636883
Samples
Known GenesANKRD29
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038041
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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