A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734068



Internal ID20510001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81582142..81582197hg38UCSC Ensembl
chr14:82048486..82048541hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734068
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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