A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612225



Internal ID20985296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166701798..166706004hg38UCSC Ensembl
chr6:167115286..167119492hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg384207
hg194207
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217038
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612225
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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