A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758304



Internal ID20534164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76231966..76231966hg38UCSC Ensembl
chr14:76698309..76698309hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758304
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