A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089662



Internal ID21998895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48300336..48300336hg38UCSC Ensembl
chr13:48874472..48874472hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604533
Samples
Known GenesLINC00441
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089662
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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