A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606390



Internal ID21798437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102150787..102150787hg38UCSC Ensembl
chr14:102617124..102617124hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091428
Supporting Variants
Samples
Known GenesWDR20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606390
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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