A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267288



Internal ID20476506
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 StatusS
Merged Variantsnsv4732040
Supporting Variants
Samples
Known GenesSLC7A2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267288
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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