A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506896



Internal ID22564844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13293441..13295176hg38UCSC Ensembl
chr8:13150950..13152685hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381736
hg191736
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854431
Supporting Variants
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506896
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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