A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060744



Internal ID19149963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:18643108..18725123hg38UCSC Ensembl
Innerchr17:18546421..18628436hg19UCSC Ensembl
Innerchr17:18487146..18569161hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3882016
hg1982016
hg1882016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560534
Samples
Known GenesFOXO3B, TBC1D28, TRIM16L, ZNF286B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060744
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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