A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413503



Internal ID21071056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45418201..45421800hg38UCSC Ensembl
chr6:45385938..45389537hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228655
Samples
Known GenesRUNX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413503
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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