A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333755



Internal ID20866935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19320005..19320522hg38UCSC Ensembl
chr1:19646499..19647016hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199849
Samples
Known GenesPQLC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333755
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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