A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396651



Internal ID21054204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53059001..53069400hg38UCSC Ensembl
chr6:52923799..52934198hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235326
Samples
Known GenesFBXO9, ICK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396651
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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