A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059766



Internal ID18802297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:47053399..47126102hg38UCSC Ensembl
Innerchr17:45130765..45203468hg19UCSC Ensembl
Innerchr17:42485764..42558467hg18UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3872704
hg1972704
hg1872704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568600
Samples
Known GenesCDC27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059766
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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