A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747329



Internal ID21386070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35195008..35196007hg38UCSC Ensembl
chr22:35591001..35592000hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433420
Supporting Variants
SamplesMDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747329
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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