A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422823



Internal ID21080376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37706328..37706816hg38UCSC Ensembl
chr8:37563846..37564334hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222360
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422823
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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