A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394548



Internal ID22452418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8009345..8014196hg38UCSC Ensembl
chr19:8074229..8079080hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384852
hg194852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940733
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394548
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