A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089117



Internal ID21998350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30625605..30625605hg38UCSC Ensembl
chr14:31094811..31094811hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610075
Samples
Known GenesSCFD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089117
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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