A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088234



Internal ID21997467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77383977..77383977hg38UCSC Ensembl
chr14:77850320..77850320hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609860
Samples
Known GenesSAMD15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088234
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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