A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067160



Internal ID18809691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82381853..82446450hg38UCSC Ensembl
Innerchr17:80339729..80404326hg19UCSC Ensembl
Innerchr17:77933018..77997615hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3864598
hg1964598
hg1864598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725173
Samples
Known GenesC17orf62, HEXDC, OGFOD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067160
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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