A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265389



Internal ID20474607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131908057..131908057hg38UCSC Ensembl
chr9:134783444..134783444hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757479
Supporting Variants
Samples
Known GenesMED27
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265389
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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