A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033307



Internal ID21942650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104905741..104906397hg38UCSC Ensembl
chr14:105372078..105372734hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614537
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033307
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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