A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438480



Internal ID21096033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121840508..121849838hg38UCSC Ensembl
chr9:124602787..124612117hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg389331
hg199331
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221969
Samples
Known GenesTTLL11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438480
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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