A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009814



Internal ID21919157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11283869..11284511hg38UCSC Ensembl
chr10:11325832..11326474hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593214
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009814
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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