A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004081



Internal ID21913424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121895298..121896093hg38UCSC Ensembl
chr9:124657577..124658372hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580780
Samples
Known GenesTTLL11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004081
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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