A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413811



Internal ID21071364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30326301..30328100hg38UCSC Ensembl
chr6:30294078..30295877hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221115
Samples
Known GenesHCG18, TRIM39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413811
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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