A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390242



Internal ID22448112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7684155..7685533hg38UCSC Ensembl
chr19:7749041..7750419hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381379
hg191379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390242
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