A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027107



Internal ID21936450
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 StatusM
Merged Variants
Supporting Variantsnssv17598347
Samples
Known GenesWDR25
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027107
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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