A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749975



Internal ID20526010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83994617..83999256hg38UCSC Ensembl
chr14:84460961..84465600hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg384640
hg194640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749975
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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