A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452763



Internal ID21110316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76058701..76068400hg38UCSC Ensembl
chr9:78673617..78683316hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg389700
hg199700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225525
Samples
Known GenesPCSK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452763
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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