A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574215



Internal ID16361624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1779718..1824004hg38UCSC Ensembl
Innerchr17:1683012..1727298hg19UCSC Ensembl
Innerchr17:1629762..1674048hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3844287
hg1944287
hg1844287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866416
Samples
Known GenesSMYD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574215
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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