A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575899



Internal ID16363308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66763470..66794392hg38UCSC Ensembl
Innerchr17:64759588..64790510hg19UCSC Ensembl
Innerchr17:62190050..62220972hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3830923
hg1930923
hg1830923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875850
Samples
Known GenesMIR634, PRKCA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575899
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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