A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751866



Internal ID20527726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31066557..31066557hg38UCSC Ensembl
chr13:31640694..31640694hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751866
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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