A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267355



Internal ID20476573
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 StatusS
Merged Variantsnsv4734817
Supporting Variants
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267355
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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