A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102811



Internal ID22012045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6544366..6544366hg38UCSC Ensembl
chr18:6544365..6544365hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634104
Samples
Known GenesC18orf64
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102811
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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