A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703624



Internal ID21375900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150366629..150366954hg38UCSC Ensembl
chr5:149746192..149746517hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392170
Supporting Variants
Samples
Known GenesTCOF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703624
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.606322


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