A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761945



Internal ID20537805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178169880..178169880hg38UCSC Ensembl
chr3:177887668..177887668hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761945
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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