A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431973



Internal ID21089526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28456701..28482900hg38UCSC Ensembl
chr9:28456699..28482898hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3826200
hg1926200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218335
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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