A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584103



Internal ID21776146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88611957..88613467hg38UCSC Ensembl
chr11:88345125..88346635hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg381511
hg191511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033569
Supporting Variants
Samples
Known GenesGRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584103
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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