A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764297



Internal ID20540157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105679140..105679140hg38UCSC Ensembl
chr12:106072918..106072918hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381111
hg191111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275116
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764297
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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