A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448714



Internal ID21106267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90638401..90647200hg38UCSC Ensembl
chr9:93400683..93409482hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222974
Samples
Known GenesDIRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448714
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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