A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767344



Internal ID20543204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119206292..119206292hg38UCSC Ensembl
chr11:119077002..119077002hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291033
Samples
Known GenesCBL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767344
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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