A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617522



Internal ID20990593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166606701..166648500hg38UCSC Ensembl
chr6:167020189..167061988hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3841800
hg1941800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217036
Samples
Known GenesRPS6KA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617522
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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