A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735116



Internal ID20511057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49820973..49821505hg38UCSC Ensembl
chr14:50287691..50288223hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267493
Samples
Known GenesNEMF
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735116
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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