A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432095



Internal ID21394097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35873214..35874213hg38UCSC Ensembl
chr14:36342420..36343419hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748783
SamplesMDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432095
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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