A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749732



Internal ID21392590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9174325..9180324hg38UCSC Ensembl
chr19:9285001..9291000hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432900
Supporting Variants
SamplesSMI041
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749732
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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