A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403968



Internal ID21061521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46770201..46773500hg38UCSC Ensembl
chr6:46737938..46741237hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231139
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403968
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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