A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747641



Internal ID21389493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129424722..129439721hg38UCSC Ensembl
chr9:132187001..132202000hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3815000
hg1915000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4435636
Supporting Variants
SamplesNB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747641
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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