A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733155



Internal ID20509082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67625686..67625749hg38UCSC Ensembl
chr14:68092403..68092466hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259189
Samples
Known GenesARG2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733155
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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