A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606839



Internal ID20979910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168694236..168927295hg38UCSC Ensembl
chr6:169094677..169327390hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38233060
hg19232714
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216119
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606839
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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