A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216546



Internal ID20783586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105174296..105195914hg38UCSC Ensembl
chr6:105622171..105643789hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3821619
hg1921619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610597
Supporting Variants
Samples
Known GenesPOPDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216546
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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