A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575898



Internal ID16363307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66414797..66522389hg38UCSC Ensembl
Innerchr17:64410915..64518507hg19UCSC Ensembl
Innerchr17:61841377..61948969hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38107593
hg19107593
hg18107593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5750n54
Supporting Variantsnssv1149791
Samples1782681117_A
Known GenesPRKCA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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