A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750657



Internal ID20526578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33052248..33052248hg38UCSC Ensembl
chr9:33052246..33052246hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265648
Samples
Known GenesSMU1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750657
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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