A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595133



Internal ID21787176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105618364..105618364hg38UCSC Ensembl
chr11:105489091..105489091hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097453
Supporting Variants
Samples
Known GenesGRIA4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595133
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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