A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748431



Internal ID21386254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:39801037..39803036hg38UCSC Ensembl
chr18:37381001..37383000hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432662
Supporting Variants
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748431
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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