A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598347



Internal ID21790391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100526650..100526758hg38UCSC Ensembl
chr14:100992987..100993095hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027107
Supporting Variants
Samples
Known GenesWDR25
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598347
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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