A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521486



Internal ID20894847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11403154..11407790hg38UCSC Ensembl
chr19:11513830..11518466hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384637
hg194637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045002
Samples
Known GenesRGL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521486
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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