A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285204



Internal ID20494422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63864752..63870950hg38UCSC Ensembl
chr14:64331470..64337668hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg386199
hg196199
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765948
Supporting Variants
Samples
Known GenesSYNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285204
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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