A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098922



Internal ID21271010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:28823239..28825614hg38UCSC Ensembl
Innerchr17:27150257..27152632hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382376
hg192376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114414
Supporting Variants
Samplessample158
Known GenesFAM222B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098922
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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