A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411785



Internal ID21069338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41788895..41793471hg38UCSC Ensembl
chr6:41756633..41761209hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg384577
hg194577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226651
Samples
Known GenesTOMM6, USP49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411785
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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