A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732040



Internal ID20507962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17552524..17552610hg38UCSC Ensembl
chr8:17410033..17410119hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267288
Samples
Known GenesSLC7A2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732040
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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