A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420660



Internal ID21078213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18731097..18752002hg38UCSC Ensembl
chr8:18588607..18609512hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3820906
hg1920906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167015
Samples
Known GenesPSD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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