A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098022



Internal ID21289295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:64618907..64624136hg38UCSC Ensembl
Innerchr17:62615025..62620254hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg385230
hg195230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110209
Supporting Variants
Samplessample45
Known GenesSMURF2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098022
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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