A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761352



Internal ID20537212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99463024..99463024hg38UCSC Ensembl
chr13:100115278..100115278hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761352
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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