A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616651



Internal ID21808698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119206303..119206303hg38UCSC Ensembl
chr11:119077013..119077013hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6087300
Supporting Variants
Samples
Known GenesCBL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616651
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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