A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422266



Internal ID21079819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11505913..11508777hg38UCSC Ensembl
chr8:11363422..11366286hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382865
hg192865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163460
Samples
Known GenesBLK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422266
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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