A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426294



Internal ID21083847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26992616..26992856hg38UCSC Ensembl
chr9:26992614..26992854hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229808
Samples
Known GenesIFT74
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426294
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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