A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083297



Internal ID21992530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17952609..17952609hg38UCSC Ensembl
chr11:17974156..17974156hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382077
hg192077
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580817
Samples
Known GenesSERGEF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083297
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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