A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749106



Internal ID20525135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74994721..74995040hg38UCSC Ensembl
chr14:75461424..75461743hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288606
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749106
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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