A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402949



Internal ID22460819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3064755..3073852hg38UCSC Ensembl
chr19:3064753..3073850hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389098
hg199098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402949
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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