A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15703619



Internal ID21375895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149021871..149022028hg38UCSC Ensembl
chr5:148401434..148401591hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392165
Supporting Variants
Samples
Known GenesSH3TC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15703619
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.439655


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