A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752348



Internal ID21390070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35249174..35250146hg38UCSC Ensembl
chr22:35645167..35646139hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38973
hg19973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4433421
Supporting Variants
SamplesNB10
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752348
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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