A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748894



Internal ID20524921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99128305..99128429hg38UCSC Ensembl
chr14:99594642..99594766hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748894
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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