A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170564



Internal ID20737604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68033059..68033403hg38UCSC Ensembl
chr8:68945294..68945638hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430531
Supporting Variants
Samples
Known GenesPREX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00058


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