A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418021



Internal ID21075574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26694001..26908700hg38UCSC Ensembl
chr9:26693999..26908698hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38214700
hg19214700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230130
Samples
Known GenesCAAP1, PLAA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418021
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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