A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703394



Internal ID21375670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14370416..14371873hg38UCSC Ensembl
chr5:14370525..14371982hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381458
hg191458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4391752
Supporting Variants
Samples
Known GenesTRIO
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703394
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00574713


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