A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429636



Internal ID21087189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:221482..492612hg38UCSC Ensembl
chr8:171482..442612hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38271131
hg19271131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223878
Samples
Known GenesFAM87A, FBXO25, RPL23AP53, TDRP, ZNF596
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429636
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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