A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284662



Internal ID20493880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6730313..6730634hg38UCSC Ensembl
chr8:6587834..6588155hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734563
Supporting Variants
Samples
Known GenesAGPAT5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284662
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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