A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416381



Internal ID21073934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8992212..8998797hg38UCSC Ensembl
chr8:8849722..8856307hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg386586
hg196586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416381
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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