A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419362



Internal ID21076915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24541670..24584482hg38UCSC Ensembl
chr9:24541668..24584480hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3842813
hg1942813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178376
Samples
Known GenesIZUMO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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