A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703652



Internal ID21375928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168967426..168967738hg38UCSC Ensembl
chr5:168394431..168394743hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392204
Supporting Variants
Samples
Known GenesSLIT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703652
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0804598


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