A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268704



Internal ID20477922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13199155..13199210hg38UCSC Ensembl
chr8:13056664..13056719hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738588
Supporting Variants
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268704
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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