A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628676



Internal ID21820723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40069083..40069163hg38UCSC Ensembl
chr17:38225336..38225416hg19UCSC Ensembl
Cytoband17q21.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021310
Supporting Variants
Samples
Known GenesTHRA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628676
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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