A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084048



Internal ID21993281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40367562..40367562hg38UCSC Ensembl
chr13:40941699..40941699hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614153
Samples
Known GenesLINC00598
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084048
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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