A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295712



Internal ID20504930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116254672..116258547hg38UCSC Ensembl
chr9:119016951..119020826hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg383876
hg193876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738439
Supporting Variants
Samples
Known GenesPAPPA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295712
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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