A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422067



Internal ID21079620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9565540..9573895hg38UCSC Ensembl
chr8:9423050..9431405hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg388356
hg198356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173735
Samples
Known GenesTNKS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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