A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749037



Internal ID21391571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80018212..80027042hg38UCSC Ensembl
chr17:77992011..78000841hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg388831
hg198831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432612
Supporting Variants
SamplesSMI018
Known GenesTBC1D16
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749037
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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