A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167921



Internal ID20734961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25941790..25944609hg38UCSC Ensembl
chr8:25799306..25802125hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg382820
hg192820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427856
Supporting Variants
Samples
Known GenesEBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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