A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752004



Internal ID21386258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34801097..34805096hg38UCSC Ensembl
chr19:35292001..35296000hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432818
Supporting Variants
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752004
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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