A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167945



Internal ID20734985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26558067..26558977hg38UCSC Ensembl
chr8:26415583..26416493hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415664
Supporting Variants
Samples
Known GenesDPYSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167945
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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