A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734817



Internal ID20510756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168967433..168967746hg38UCSC Ensembl
chr5:168394438..168394751hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267355
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734817
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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