A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764755



Internal ID20540615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69632080..69632080hg38UCSC Ensembl
chr12:70025860..70025860hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259132
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764755
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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