A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767841



Internal ID20543701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15737520..15737520hg38UCSC Ensembl
chr3:15779027..15779027hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261049
Samples
Known GenesANKRD28
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767841
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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