A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748307



Internal ID21387272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31192095..31211094hg38UCSC Ensembl
chr19:31683001..31702000hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3819000
hg1919000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432810
Supporting Variants
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748307
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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