A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085131



Internal ID21994364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23695641..23695641hg38UCSC Ensembl
chr14:24164850..24164850hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085131
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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