A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225155



Internal ID20792195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13109279..13109653hg38UCSC Ensembl
chr8:12966788..12967162hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38375
hg19375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434290
Supporting Variants
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225155
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00029


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