A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094762



Internal ID22003995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64822374..64822374hg38UCSC Ensembl
chr14:65289092..65289092hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612463
Samples
Known GenesSPTB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094762
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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