A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023023



Internal ID21932366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77379411..77390030hg38UCSC Ensembl
chr14:77845754..77856373hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3810620
hg1910620
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615447
Samples
Known GenesSAMD15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023023
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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