A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745111



Internal ID20521116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104061813..104061883hg38UCSC Ensembl
chr12:104455591..104455661hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745111
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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