A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106822



Internal ID22016055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63865405..63870589hg38UCSC Ensembl
chr14:64332123..64337307hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg385185
hg195185
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599817
Samples
Known GenesSYNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106822
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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