A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618126



Internal ID20991197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110763274..110763861hg38UCSC Ensembl
chr6:111084477..111085064hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216806
Samples
Known GenesCDK19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618126
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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