A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16273442



Internal ID20482660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124586199..124586199hg38UCSC Ensembl
chr11:124456095..124456095hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750795
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16273442
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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