A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165665



Internal ID20732705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13194659..13203417hg38UCSC Ensembl
chr8:13052168..13060926hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg388759
hg198759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424736
Supporting Variants
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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