A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392204



Internal ID21383234
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 StatusM
Merged Variants
Supporting Variantsnssv15703652
Samples
Known GenesSLIT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392204
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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