A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432613



Internal ID21394615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80018243..80027063hg38UCSC Ensembl
chr17:77992042..78000862hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg388821
hg198821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv327n172
Supporting Variantsnssv15752131
SamplesMDQ045
Known GenesTBC1D16
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432613
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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