A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267805



Internal ID20477023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93420969..93427029hg38UCSC Ensembl
chr11:93154135..93160195hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386061
hg196061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733434
Supporting Variants
Samples
Known GenesCCDC67
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267805
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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