A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426535



Internal ID21084088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36206238..36229032hg38UCSC Ensembl
chr8:36063756..36086550hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3822795
hg1922795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426535
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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