A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096981



Internal ID22006214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52801383..52801383hg38UCSC Ensembl
chr14:53268101..53268101hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg383028
hg193028
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096981
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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