A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417624



Internal ID21075177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25674201..25680800hg38UCSC Ensembl
chr9:25674199..25680798hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7661n223
Supporting Variantsnssv18236098
Samples
Known GenesTUSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417624
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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