A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396760



Internal ID21054313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28952470..29380836hg38UCSC Ensembl
chr6:28920247..29348613hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38428367
hg19428367
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221187
Samples
Known GenesLOC100129636, OR12D3, OR14J1, OR2B3, OR2J2, OR2J3, OR2W1, OR5V1, ZNF311
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396760
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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