A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744802



Internal ID20520805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:100636574..100637270hg38UCSC Ensembl
chr12:101030352..101031048hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273843
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744802
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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