A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039666



Internal ID21949009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69406908..69407006hg38UCSC Ensembl
chr14:69873625..69873723hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613467
Samples
Known GenesSLC39A9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039666
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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