A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435006



Internal ID21092559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16420401..16673800hg38UCSC Ensembl
chr8:16277910..16531309hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38253400
hg19253400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435006
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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