A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420437



Internal ID21077990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27034471..27131267hg38UCSC Ensembl
chr9:27034469..27131265hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3896797
hg1996797
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236068
Samples
Known GenesIFT74, TEK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420437
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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