A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404014



Internal ID22461884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10230560..10230613hg38UCSC Ensembl
chr19:10341236..10341289hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945670
Supporting Variants
Samples
Known GenesS1PR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404014
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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