A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408266



Internal ID21065819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28882481..28920690hg38UCSC Ensembl
chr6:28850258..28888467hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3838210
hg1938210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232124
Samples
Known GenesHCG14, TRIM27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408266
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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