A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324879



Internal ID20858009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93222943..93224782hg38UCSC Ensembl
chr1:93688500..93690339hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg381840
hg191840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203182
Samples
Known GenesCCDC18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324879
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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