A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762142



Internal ID20538002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9106892..9106892hg38UCSC Ensembl
chr11:9128439..9128439hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382543
hg192543
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762142
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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