A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094549



Internal ID22003782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24406248..24406248hg38UCSC Ensembl
chr14:24875454..24875454hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604990
Samples
Known GenesNYNRIN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094549
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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