A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391751



Internal ID21382781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13855192..13855506hg38UCSC Ensembl
chr5:13855301..13855615hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703392
Samples
Known GenesDNAH5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391751
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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