A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427236



Internal ID21084789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53871706..53921743hg38UCSC Ensembl
chr8:54784266..54834303hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3850038
hg1950038
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223941
Samples
Known GenesRGS20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427236
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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