A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092723



Internal ID22001956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78179983..78179983hg38UCSC Ensembl
chr11:77891029..77891029hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579978
Samples
Known GenesKCTD21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092723
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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