A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038286



Internal ID21947629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93894049..93894123hg38UCSC Ensembl
chr14:94360395..94360469hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038286
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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