A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143068



Internal ID342269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93420600..93426896hg38UCSC Ensembl
chr11:93153766..93160062hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386297
hg196297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052063
Samples
Known GenesCCDC67
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143068
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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