A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614753



Internal ID21806800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121221297..121221297hg38UCSC Ensembl
chr11:121092006..121092006hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088930
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614753
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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