A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087830



Internal ID21997063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85643354..85643354hg38UCSC Ensembl
chr14:86109698..86109698hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609713
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087830
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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