A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766800



Internal ID20542660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2643289..2643289hg38UCSC Ensembl
chr19:2643287..2643287hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260183
Samples
Known GenesGNG7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766800
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