A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088655



Internal ID21997888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95293273..95293273hg38UCSC Ensembl
chr14:95759610..95759610hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609564
Samples
Known GenesCLMN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088655
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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