A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604990



Internal ID21797037
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 StatusS
Merged Variantsnsv6094549
Supporting Variants
Samples
Known GenesNYNRIN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604990
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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