A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765948



Internal ID20541808
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 StatusM
Merged Variants
Supporting Variantsnssv16285204
Samples
Known GenesSYNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765948
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer