A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748593



Internal ID21386279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:296001..383000hg38UCSC Ensembl
chr6:296001..383000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3887000
hg1987000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434900
Supporting Variants
SamplesMDQ010
Known GenesDUSP22
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748593
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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