A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416862



Internal ID21074415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:111555055..111710524hg38UCSC Ensembl
chr8:112567284..112722753hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38155470
hg19155470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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