A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038450



Internal ID21947793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31455681..31455782hg38UCSC Ensembl
chr14:31924887..31924988hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609242
Samples
Known GenesDTD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038450
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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