A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432830



Internal ID21394832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41842797..41843906hg38UCSC Ensembl
chr19:42346881..42347973hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381110
hg191093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15754042
SamplesMDQ010
Known GenesLYPD4
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432830
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