A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763272



Internal ID20539132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86909217..86909217hg38UCSC Ensembl
chr14:87375561..87375561hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294712
Samples
Known GenesLOC283585
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763272
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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