A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422062



Internal ID21079615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11768840..11780100hg38UCSC Ensembl
chr8:11626349..11637609hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3811261
hg1911261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163799
Samples
Known GenesNEIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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