A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433866



Internal ID21091419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8922360..8937713hg38UCSC Ensembl
chr8:8779870..8795223hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3815354
hg1915354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433866
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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