A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267425



Internal ID20476643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11464572..11464796hg38UCSC Ensembl
chr19:11575387..11575611hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741713
Supporting Variants
Samples
Known GenesELAVL3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267425
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