A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333816



Internal ID20866997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212401401..212422800hg38UCSC Ensembl
chr1:212574743..212596142hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3821400
hg1921400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199952
Samples
Known GenesTMEM206
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333816
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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