A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398722



Internal ID21056275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46009801..46023400hg38UCSC Ensembl
chr6:45977538..45991137hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3813600
hg1913600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229976
Samples
Known GenesCLIC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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