A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098073



Internal ID21290681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54609874..54614067hg38UCSC Ensembl
Innerchr17:52687235..52691428hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg384194
hg194194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113760
Supporting Variants
Samplessample62
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098073
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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