A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092765



Internal ID22001998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26661882..26661882hg38UCSC Ensembl
chr14:27131088..27131088hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092765
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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