A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703455



Internal ID21375731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:40982041..40985442hg38UCSC Ensembl
chr5:40982143..40985544hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg383402
hg193402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391867
Supporting Variants
Samples
Known GenesC7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703455
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00862069


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