A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092911



Internal ID22002144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81811650..81811650hg38UCSC Ensembl
chr14:82277994..82277994hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092911
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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