A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768078



Internal ID20543938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36536940..36536940hg38UCSC Ensembl
chr11:36558490..36558490hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg385969
hg195969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768078
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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