A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275942



Internal ID20485160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65676392..65676392hg38UCSC Ensembl
chr11:65443863..65443863hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755186
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275942
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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