A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618364



Internal ID20991435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134876873..134877263hg38UCSC Ensembl
chr6:135198011..135198401hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618364
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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